ClinVar Miner

List of variants reported as likely pathogenic for Hereditary diffuse gastric adenocarcinoma by Myriad Genetics, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 79
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.1566-1G>C rs113583899 0.00001
NM_001903.5(CTNNA1):c.105+1G>C rs374313094
NM_001903.5(CTNNA1):c.1390-6_1392delinsA
NM_001903.5(CTNNA1):c.1899+1G>C rs1580862601
NM_001903.5(CTNNA1):c.1991dup (p.Ala665fs) rs1764809610
NM_001903.5(CTNNA1):c.1997del (p.Gly666fs) rs1181915653
NM_001903.5(CTNNA1):c.2008dup (p.Arg670fs)
NM_001903.5(CTNNA1):c.2017_2018dup (p.Met673fs)
NM_001903.5(CTNNA1):c.468+1G>T
NM_004360.5(CDH1):c.1008+1G>T rs1960844889
NM_004360.5(CDH1):c.1008+2_1008+4del
NM_004360.5(CDH1):c.1008G>A (p.Glu336=) rs267606712
NM_004360.5(CDH1):c.1128_1137+1delinsGGAGT
NM_004360.5(CDH1):c.1137+2T>A
NM_004360.5(CDH1):c.1137G>A (p.Thr379=) rs587783050
NM_004360.5(CDH1):c.1137G>T (p.Thr379=) rs587783050
NM_004360.5(CDH1):c.1298_1320+12del
NM_004360.5(CDH1):c.1320+1G>A
NM_004360.5(CDH1):c.1320+1G>C rs886039685
NM_004360.5(CDH1):c.1321-1G>T
NM_004360.5(CDH1):c.1321-6_1324del
NM_004360.5(CDH1):c.1321-9_1331dup
NM_004360.5(CDH1):c.139_163+18del
NM_004360.5(CDH1):c.152_163+11del
NM_004360.5(CDH1):c.1565+1G>A rs587780113
NM_004360.5(CDH1):c.1565+1G>C rs587780113
NM_004360.5(CDH1):c.1565+1G>T rs587780113
NM_004360.5(CDH1):c.1565+1del rs1064795267
NM_004360.5(CDH1):c.1565+2dup rs1555516200
NM_004360.5(CDH1):c.1566-2A>G rs1555516520
NM_004360.5(CDH1):c.163+2T>C
NM_004360.5(CDH1):c.164-1G>A rs1597884512
NM_004360.5(CDH1):c.164-21_288del
NM_004360.5(CDH1):c.164-2A>G rs2152126585
NM_004360.5(CDH1):c.1679C>G (p.Thr560Arg) rs746481984
NM_004360.5(CDH1):c.1711+1G>A rs886041161
NM_004360.5(CDH1):c.1711+1G>T
NM_004360.5(CDH1):c.1711+1dup rs2152137028
NM_004360.5(CDH1):c.1711+2_1711+7del rs786203089
NM_004360.5(CDH1):c.1901C>T (p.Ala634Val) rs121964878
NM_004360.5(CDH1):c.1936+1G>A rs2152138630
NM_004360.5(CDH1):c.1A>G (p.Met1Val) rs1555509622
NM_004360.5(CDH1):c.2164+1G>A
NM_004360.5(CDH1):c.2164+1G>C rs1961238458
NM_004360.5(CDH1):c.2164+1_2164+2del
NM_004360.5(CDH1):c.2164+1del
NM_004360.5(CDH1):c.2164+5G>A
NM_004360.5(CDH1):c.2165-1G>C rs1385720097
NM_004360.5(CDH1):c.2165-1G>T rs1385720097
NM_004360.5(CDH1):c.2165-2A>G rs1596970624
NM_004360.5(CDH1):c.2195G>A (p.Arg732Gln) rs1060501244
NM_004360.5(CDH1):c.2295+1G>A
NM_004360.5(CDH1):c.2295+1G>C rs1596971108
NM_004360.5(CDH1):c.2296-2A>G rs876660393
NM_004360.5(CDH1):c.2296-3A>G rs113067020
NM_004360.5(CDH1):c.2440-2A>G rs1555518210
NM_004360.5(CDH1):c.2461_2467del (p.Asp821fs)
NM_004360.5(CDH1):c.2488_2489dup (p.Leu831fs)
NM_004360.5(CDH1):c.2505_2506dup (p.Glu836fs) rs1555518236
NM_004360.5(CDH1):c.2T>C (p.Met1Thr) rs1555509623
NM_004360.5(CDH1):c.2T>G (p.Met1Arg) rs1555509623
NM_004360.5(CDH1):c.3G>A (p.Met1Ile) rs878854691
NM_004360.5(CDH1):c.49-1G>T
NM_004360.5(CDH1):c.49-2A>G rs1060501226
NM_004360.5(CDH1):c.531+1G>A rs1131690808
NM_004360.5(CDH1):c.531+1G>C rs1131690808
NM_004360.5(CDH1):c.531+1G>T rs1131690808
NM_004360.5(CDH1):c.531+2T>C
NM_004360.5(CDH1):c.532-1G>C rs771085839
NM_004360.5(CDH1):c.532-2A>C
NM_004360.5(CDH1):c.532-2A>G
NM_004360.5(CDH1):c.687+1G>A rs1567504977
NM_004360.5(CDH1):c.687+1G>C rs1567504977
NM_004360.5(CDH1):c.687+1G>T rs1567504977
NM_004360.5(CDH1):c.715G>A (p.Gly239Arg) rs587780537
NM_004360.5(CDH1):c.832+1G>A rs878854697
NM_004360.5(CDH1):c.832+1G>T rs878854697
NM_004360.5(CDH1):c.833-2A>C
NM_004360.5(CDH1):c.833-2A>G rs1555515596

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.