ClinVar Miner

List of variants reported as pathogenic for diffuse type adenocarcinoma by Myriad Genetics, Inc.

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 256
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001903.5(CTNNA1):c.385C>T (p.Arg129Ter) rs758599826 0.00001
NM_004360.5(CDH1):c.1003C>T (p.Arg335Ter) rs587780784 0.00001
NC_000016.10:g.68815516del rs2152134667
NM_001903.5(CTNNA1):c.1006del (p.Glu336fs)
NM_001903.5(CTNNA1):c.1046C>A (p.Ser349Ter)
NM_001903.5(CTNNA1):c.1075G>T (p.Glu359Ter)
NM_001903.5(CTNNA1):c.1078_1081del (p.Arg360fs) rs1753991365
NM_001903.5(CTNNA1):c.1246_1249del (p.Val416fs) rs1426385729
NM_001903.5(CTNNA1):c.1292_1295del (p.Ile431fs) rs1754363697
NM_001903.5(CTNNA1):c.1325_1328del (p.Asn442fs)
NM_001903.5(CTNNA1):c.1330dup (p.Glu444fs) rs1758714268
NM_001903.5(CTNNA1):c.1351C>T (p.Arg451Ter) rs201498915
NM_001903.5(CTNNA1):c.1430_1433del (p.Ser477fs)
NM_001903.5(CTNNA1):c.1450dup (p.Met484fs)
NM_001903.5(CTNNA1):c.1464dup (p.Glu489fs)
NM_001903.5(CTNNA1):c.1473G>A (p.Trp491Ter)
NM_001903.5(CTNNA1):c.1474dup (p.Glu492fs)
NM_001903.5(CTNNA1):c.1480C>T (p.Gln494Ter)
NM_001903.5(CTNNA1):c.151_152del (p.Lys51fs) rs2149656252
NM_001903.5(CTNNA1):c.1544C>G (p.Ser515Ter) rs1762138459
NM_001903.5(CTNNA1):c.157_158del (p.Gly53fs)
NM_001903.5(CTNNA1):c.1581dup (p.Ile528fs) rs2150288001
NM_001903.5(CTNNA1):c.1613_1617dup (p.Arg540fs) rs1580854940
NM_001903.5(CTNNA1):c.1636C>T (p.Arg546Ter) rs1763609978
NM_001903.5(CTNNA1):c.1636del (p.Arg546fs)
NM_001903.5(CTNNA1):c.1815del (p.Met606fs)
NM_001903.5(CTNNA1):c.1822G>T (p.Glu608Ter)
NM_001903.5(CTNNA1):c.1904_1905del (p.Pro635fs)
NM_001903.5(CTNNA1):c.1906del (p.Glu636fs)
NM_001903.5(CTNNA1):c.1928_1929del (p.Asp642_Phe643insTer)
NM_001903.5(CTNNA1):c.1969C>T (p.Gln657Ter) rs1764805365
NM_001903.5(CTNNA1):c.2023C>T (p.Gln675Ter) rs1580907792
NM_001903.5(CTNNA1):c.214_215del (p.Phe72fs)
NM_001903.5(CTNNA1):c.222_223del (p.Lys75fs) rs1580984414
NM_001903.5(CTNNA1):c.292C>T (p.Arg98Ter) rs773235871
NM_001903.5(CTNNA1):c.361C>T (p.Arg121Ter) rs1043413100
NM_001903.5(CTNNA1):c.382dup (p.Ala128fs)
NM_001903.5(CTNNA1):c.39G>A (p.Trp13Ter)
NM_001903.5(CTNNA1):c.406dup (p.Thr136fs) rs1581105774
NM_001903.5(CTNNA1):c.580del (p.Arg194fs)
NM_001903.5(CTNNA1):c.608_623del (p.His203fs)
NM_001903.5(CTNNA1):c.660_666del (p.Tyr222fs)
NM_001903.5(CTNNA1):c.68dup (p.Ala24fs) rs2149651992
NM_001903.5(CTNNA1):c.739C>T (p.Gln247Ter)
NM_001903.5(CTNNA1):c.86del (p.Leu29fs) rs745411817
NM_001903.5(CTNNA1):c.892G>T (p.Glu298Ter)
NM_001903.5(CTNNA1):c.919del (p.Glu307fs) rs1760848495
NM_001903.5(CTNNA1):c.99del (p.Thr34fs)
NM_004360.5(CDH1):c.1009_1010del (p.Ser337Phefs) rs786201045
NM_004360.5(CDH1):c.1020_1051del (p.Tyr341fs)
NM_004360.5(CDH1):c.1040_1041dup (p.Ala348fs)
NM_004360.5(CDH1):c.1051C>T (p.Gln351Ter) rs1555515726
NM_004360.5(CDH1):c.1062dup (p.Leu355fs)
NM_004360.5(CDH1):c.1064del (p.Gly354_Leu355insTer) rs1555515731
NM_004360.5(CDH1):c.1064dup (p.Leu355fs) rs1555515731
NM_004360.5(CDH1):c.1078del (p.Thr360fs)
NM_004360.5(CDH1):c.1091_1092del (p.Thr364fs)
NM_004360.5(CDH1):c.1097_1112del (p.Thr366fs)
NM_004360.5(CDH1):c.1098_1099insAA (p.Asp367fs)
NM_004360.5(CDH1):c.1098_1101del (p.Asp367fs)
NM_004360.5(CDH1):c.1123_1129del (p.Phe375fs)
NM_004360.5(CDH1):c.1131del (p.Thr378fs) rs1131690812
NM_004360.5(CDH1):c.1143_1145delinsA (p.Gly382fs)
NM_004360.5(CDH1):c.1145del (p.Gly382fs) rs1555515863
NM_004360.5(CDH1):c.1155dup (p.Glu386Ter)
NM_004360.5(CDH1):c.1162G>T (p.Glu388Ter)
NM_004360.5(CDH1):c.11G>A (p.Trp4Ter) rs1962423346
NM_004360.5(CDH1):c.1212del (p.Asn405fs) rs1597895871
NM_004360.5(CDH1):c.1212dup (p.Asn405fs) rs1597895871
NM_004360.5(CDH1):c.1222dup (p.Ala408fs)
NM_004360.5(CDH1):c.1226G>A (p.Trp409Ter)
NM_004360.5(CDH1):c.1228G>T (p.Glu410Ter)
NM_004360.5(CDH1):c.1234_1235dup (p.Ile415fs) rs1567507825
NM_004360.5(CDH1):c.124_126delinsT (p.Pro42fs) rs876658865
NM_004360.5(CDH1):c.1273del (p.Val425fs)
NM_004360.5(CDH1):c.1295_1296delinsTTTT (p.Asn432fs)
NM_004360.5(CDH1):c.1301del (p.Gly434fs)
NM_004360.5(CDH1):c.1312del (p.Thr438fs) rs1555515920
NM_004360.5(CDH1):c.1315_1316delinsCAA (p.Ala439fs)
NM_004360.5(CDH1):c.1338_1345del (p.Lys447fs)
NM_004360.5(CDH1):c.1340_1346del (p.Lys447fs)
NM_004360.5(CDH1):c.1342C>T (p.Gln448Ter)
NM_004360.5(CDH1):c.1343dup (p.Gln449fs)
NM_004360.5(CDH1):c.1350C>G (p.Tyr450Ter)
NM_004360.5(CDH1):c.1354_1357del (p.Leu452fs) rs886039612
NM_004360.5(CDH1):c.1369del (p.Thr457fs) rs1960959718
NM_004360.5(CDH1):c.136del (p.Leu46fs)
NM_004360.5(CDH1):c.137del (p.Leu46fs)
NM_004360.5(CDH1):c.1380del (p.Pro461fs) rs1567508847
NM_004360.5(CDH1):c.1386del (p.Phe462fs)
NM_004360.5(CDH1):c.1397_1398del (p.Leu466fs) rs1597897893
NM_004360.5(CDH1):c.1438_1453del (p.Val480fs)
NM_004360.5(CDH1):c.1450_1463del (p.Pro484fs)
NM_004360.5(CDH1):c.1467del (p.Glu490fs)
NM_004360.5(CDH1):c.1476_1477del (p.Arg492fs) rs876659208
NM_004360.5(CDH1):c.1480G>T (p.Glu494Ter) rs778871891
NM_004360.5(CDH1):c.1488_1494del (p.Glu497fs) rs876658261
NM_004360.5(CDH1):c.1489G>T (p.Glu497Ter)
NM_004360.5(CDH1):c.1492del (p.Asp498fs)
NM_004360.5(CDH1):c.1531C>T (p.Gln511Ter) rs1131690810
NM_004360.5(CDH1):c.1541_1565delinsTGTAGT (p.Asp514_Thr522delinsValTer)
NM_004360.5(CDH1):c.1543dup (p.Thr515fs)
NM_004360.5(CDH1):c.1544_1545del (p.Thr515fs)
NM_004360.5(CDH1):c.1555C>T (p.Gln519Ter)
NM_004360.5(CDH1):c.1569T>A (p.Tyr523Ter) rs876659716
NM_004360.5(CDH1):c.1569T>G (p.Tyr523Ter) rs876659716
NM_004360.5(CDH1):c.1577G>A (p.Trp526Ter) rs1596960298
NM_004360.5(CDH1):c.1578G>A (p.Trp526Ter) rs886039590
NM_004360.5(CDH1):c.1582_1583del (p.Asp528fs)
NM_004360.5(CDH1):c.1587dup (p.Ala530fs) rs1555516532
NM_004360.5(CDH1):c.1590dup (p.Asn531fs) rs1555516535
NM_004360.5(CDH1):c.1595G>A (p.Trp532Ter) rs1596960368
NM_004360.5(CDH1):c.1600dup (p.Glu534fs)
NM_004360.5(CDH1):c.1605del (p.Asn536fs) rs1596960393
NM_004360.5(CDH1):c.1629del (p.Thr544fs)
NM_004360.5(CDH1):c.1660G>T (p.Glu554Ter)
NM_004360.5(CDH1):c.1679dup (p.Tyr561fs) rs1555516567
NM_004360.5(CDH1):c.1682dup (p.Tyr561Ter)
NM_004360.5(CDH1):c.1689_1694delinsACGTA (p.Leu564fs)
NM_004360.5(CDH1):c.1710del (p.Asn570fs) rs1961081411
NM_004360.5(CDH1):c.172G>T (p.Glu58Ter)
NM_004360.5(CDH1):c.1746dup (p.Leu583fs) rs1131690817
NM_004360.5(CDH1):c.1779del (p.Ile594fs) rs876661118
NM_004360.5(CDH1):c.1779dup (p.Ile594fs) rs876661118
NM_004360.5(CDH1):c.1792C>T (p.Arg598Ter) rs121964877
NM_004360.5(CDH1):c.1795del (p.Thr599fs)
NM_004360.5(CDH1):c.1828C>T (p.Gln610Ter)
NM_004360.5(CDH1):c.1840del (p.Ile614fs)
NM_004360.5(CDH1):c.1878_1885del (p.Phe626fs) rs2152138505
NM_004360.5(CDH1):c.187C>T (p.Arg63Ter) rs587783047
NM_004360.5(CDH1):c.1889del (p.Leu630fs)
NM_004360.5(CDH1):c.1893dup (p.His632fs) rs1596963827
NM_004360.5(CDH1):c.1895_1896del (p.His632fs) rs1060501224
NM_004360.5(CDH1):c.1913G>A (p.Trp638Ter) rs1567512585
NM_004360.5(CDH1):c.1914G>A (p.Trp638Ter) rs1961170989
NM_004360.5(CDH1):c.1921C>T (p.Gln641Ter) rs587782750
NM_004360.5(CDH1):c.1928del (p.Asn643fs)
NM_004360.5(CDH1):c.1935_1936+9del
NM_004360.5(CDH1):c.1939C>T (p.Gln647Ter) rs778195664
NM_004360.5(CDH1):c.1942G>T (p.Glu648Ter) rs971882211
NM_004360.5(CDH1):c.1948_1949del (p.Ile650fs) rs1555517074
NM_004360.5(CDH1):c.1955dup (p.Leu652fs)
NM_004360.5(CDH1):c.1979dup (p.Gly661_Asp662insTer) rs730881653
NM_004360.5(CDH1):c.1982del (p.Gly661fs) rs1596965628
NM_004360.5(CDH1):c.1993del (p.Ile665fs) rs1567513227
NM_004360.5(CDH1):c.1999del (p.Leu667fs) rs786202033
NM_004360.5(CDH1):c.2029dup (p.Gln677fs) rs1555517100
NM_004360.5(CDH1):c.202del (p.Tyr68fs) rs786202151
NM_004360.5(CDH1):c.2049_2056del (p.Val683_Ser684insTer)
NM_004360.5(CDH1):c.2064_2065del (p.Cys688_Glu689delinsTer) rs587781276
NM_004360.5(CDH1):c.2095C>T (p.Gln699Ter) rs121964874
NM_004360.5(CDH1):c.2100del (p.Val701fs) rs1555517136
NM_004360.5(CDH1):c.2114del (p.Leu705fs)
NM_004360.5(CDH1):c.2144del (p.Gly715fs) rs1555517153
NM_004360.5(CDH1):c.2200A>T (p.Arg734Ter)
NM_004360.5(CDH1):c.220C>T (p.Arg74Ter) rs876658932
NM_004360.5(CDH1):c.2220del (p.Leu741fs)
NM_004360.5(CDH1):c.2222T>G (p.Leu741Ter)
NM_004360.5(CDH1):c.2275G>T (p.Gly759Ter)
NM_004360.5(CDH1):c.2276del (p.Gly759fs) rs1555517680
NM_004360.5(CDH1):c.2287G>T (p.Glu763Ter) rs587780787
NM_004360.5(CDH1):c.228dup (p.Val77fs)
NM_004360.5(CDH1):c.2293C>T (p.Gln765Ter) rs876658575
NM_004360.5(CDH1):c.2293dup (p.Gln765fs)
NM_004360.5(CDH1):c.2296-1G>A rs1057517542
NM_004360.5(CDH1):c.2297_2307delinsTTGA (p.Asp766fs)
NM_004360.5(CDH1):c.2301del (p.Phe767fs)
NM_004360.5(CDH1):c.2311C>T (p.Gln771Ter) rs1131690813
NM_004360.5(CDH1):c.2351_2352del (p.Arg784fs)
NM_004360.5(CDH1):c.2355_2356insCAACCCTCATGGT (p.Asp786delinsGlnProSerTrpTer)
NM_004360.5(CDH1):c.2386dup (p.Arg796fs) rs1375617541
NM_004360.5(CDH1):c.2398del (p.Arg800fs) rs587783048
NM_004360.5(CDH1):c.2416G>T (p.Glu806Ter)
NM_004360.5(CDH1):c.2422G>T (p.Gly808Ter)
NM_004360.5(CDH1):c.2430del (p.Phe810fs) rs786203752
NM_004360.5(CDH1):c.244_248del (p.Val82fs)
NM_004360.5(CDH1):c.2474dup (p.Pro826fs) rs1555518221
NM_004360.5(CDH1):c.247delinsGTGTGG (p.Ile83fs)
NM_004360.5(CDH1):c.2480dup (p.Tyr827Ter) rs1596976243
NM_004360.5(CDH1):c.259dup (p.Arg87fs)
NM_004360.5(CDH1):c.25_26del (p.Ser9fs)
NM_004360.5(CDH1):c.261del (p.Arg87fs) rs1555514429
NM_004360.5(CDH1):c.267dup (p.Arg90fs)
NM_004360.5(CDH1):c.26C>A (p.Ser9Ter) rs1555509646
NM_004360.5(CDH1):c.283C>T (p.Gln95Ter) rs781409616
NM_004360.5(CDH1):c.294delinsTT (p.Leu99fs)
NM_004360.5(CDH1):c.301_314del (p.Tyr101fs)
NM_004360.5(CDH1):c.303C>G (p.Tyr101Ter)
NM_004360.5(CDH1):c.309G>A (p.Trp103Ter) rs2152126900
NM_004360.5(CDH1):c.315del (p.Thr106fs) rs1064795703
NM_004360.5(CDH1):c.321C>G (p.Tyr107Ter) rs765929630
NM_004360.5(CDH1):c.326del (p.Lys109fs)
NM_004360.5(CDH1):c.331del (p.Ser111fs)
NM_004360.5(CDH1):c.333del (p.Thr112fs)
NM_004360.5(CDH1):c.360dup (p.His121fs) rs878854690
NM_004360.5(CDH1):c.376_382del (p.Pro126fs)
NM_004360.5(CDH1):c.376_382dup (p.His128fs) rs1567501500
NM_004360.5(CDH1):c.377del (p.Pro126fs) rs1060501215
NM_004360.5(CDH1):c.377dup (p.Pro127fs) rs1060501215
NM_004360.5(CDH1):c.382del (p.His128fs) rs1555514492
NM_004360.5(CDH1):c.384dup (p.Gln129fs)
NM_004360.5(CDH1):c.385C>T (p.Gln129Ter)
NM_004360.5(CDH1):c.414_415dup (p.Leu139fs)
NM_004360.5(CDH1):c.419_420del (p.Leu140fs)
NM_004360.5(CDH1):c.42dup (p.Leu15fs)
NM_004360.5(CDH1):c.438_439del (p.Pro147fs) rs1555515197
NM_004360.5(CDH1):c.454_460del (p.Gln152fs) rs1131690815
NM_004360.5(CDH1):c.454_460dup (p.Arg154fs) rs1131690815
NM_004360.5(CDH1):c.455_465del (p.Gln152fs) rs1555515210
NM_004360.5(CDH1):c.456_457delinsTT (p.Gln152_Lys153delinsHisTer)
NM_004360.5(CDH1):c.464_467dup (p.Trp156Ter)
NM_004360.5(CDH1):c.46C>T (p.Gln16Ter)
NM_004360.5(CDH1):c.47dup (p.Val17fs)
NM_004360.5(CDH1):c.480_486delinsAGAATA (p.Ile161fs) rs1555515217
NM_004360.5(CDH1):c.484_485delinsT (p.Cys163fs)
NM_004360.5(CDH1):c.504del (p.Gly169fs) rs864622655
NM_004360.5(CDH1):c.506del (p.Gly169fs)
NM_004360.5(CDH1):c.521dup (p.Asn174fs) rs587781290
NM_004360.5(CDH1):c.553G>T (p.Glu185Ter)
NM_004360.5(CDH1):c.570C>G (p.Tyr190Ter)
NM_004360.5(CDH1):c.59G>A (p.Trp20Ter) rs121964875
NM_004360.5(CDH1):c.602_603del (p.Pro201fs)
NM_004360.5(CDH1):c.602dup (p.Val202fs)
NM_004360.5(CDH1):c.603del (p.Val202fs) rs1131690809
NM_004360.5(CDH1):c.60G>A (p.Trp20Ter) rs786203576
NM_004360.5(CDH1):c.628G>T (p.Glu210Ter)
NM_004360.5(CDH1):c.632_633del (p.Thr211fs)
NM_004360.5(CDH1):c.634G>T (p.Gly212Ter)
NM_004360.5(CDH1):c.638G>A (p.Trp213Ter)
NM_004360.5(CDH1):c.639G>A (p.Trp213Ter)
NM_004360.5(CDH1):c.640del (p.Trp213_Leu214insTer)
NM_004360.5(CDH1):c.64_80del (p.Cys22fs)
NM_004360.5(CDH1):c.656del (p.Pro219fs) rs1555515284
NM_004360.5(CDH1):c.67C>T (p.Gln23Ter) rs1962456814
NM_004360.5(CDH1):c.696_697del (p.His233fs) rs1060501214
NM_004360.5(CDH1):c.696_750del (p.His233fs)
NM_004360.5(CDH1):c.698dup (p.His233fs)
NM_004360.5(CDH1):c.720del (p.Asn240fs) rs1131690819
NM_004360.5(CDH1):c.737_760delinsGGGC (p.Met246fs)
NM_004360.5(CDH1):c.763C>T (p.Gln255Ter)
NM_004360.5(CDH1):c.76G>T (p.Glu26Ter) rs786201058
NM_004360.5(CDH1):c.807dup (p.Ser270fs)
NM_004360.5(CDH1):c.817G>T (p.Glu273Ter)
NM_004360.5(CDH1):c.81del (p.Cys28fs)
NM_004360.5(CDH1):c.830del (p.Pro277fs)
NM_004360.5(CDH1):c.846_847delinsTT (p.Met282_Glu283delinsIleTer)
NM_004360.5(CDH1):c.84C>A (p.Cys28Ter)
NM_004360.5(CDH1):c.878dup (p.Asn294fs)
NM_004360.5(CDH1):c.885del (p.Tyr296fs)
NM_004360.5(CDH1):c.888C>G (p.Tyr296Ter)
NM_004360.5(CDH1):c.919C>T (p.Gln307Ter)
NM_004360.5(CDH1):c.943_944del (p.Asn315fs) rs2152132067
NM_004360.5(CDH1):c.943_946del (p.Asn315fs)
NM_004360.5(CDH1):c.944del (p.Asn315fs)
NM_004360.5(CDH1):c.968del (p.Thr323fs)
NM_004360.5(CDH1):c.970G>T (p.Gly324Ter)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.