ClinVar Miner

List of variants in gene CDH1 reported as uncertain significance for breast carcinoma

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 153
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.2635G>A (p.Gly879Ser) rs200911775 0.00013
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly) rs121964872 0.00011
NM_004360.5(CDH1):c.2644G>A (p.Asp882Asn) rs200104963 0.00009
NM_004360.5(CDH1):c.854C>T (p.Thr285Ile) rs587781634 0.00007
NM_004360.5(CDH1):c.846G>A (p.Met282Ile) rs200932258 0.00006
NM_004360.5(CDH1):c.1793G>A (p.Arg598Gln) rs780759537 0.00004
NM_004360.5(CDH1):c.2249A>G (p.Asp750Gly) rs759608783 0.00004
NM_004360.5(CDH1):c.2336G>A (p.Arg779Gln) rs587781311 0.00004
NM_004360.5(CDH1):c.2450C>T (p.Ala817Val) rs587782024 0.00004
NM_004360.5(CDH1):c.2474C>T (p.Pro825Leu) rs587781312 0.00004
NM_004360.5(CDH1):c.377C>T (p.Pro126Leu) rs746703615 0.00004
NM_004360.5(CDH1):c.1417G>A (p.Val473Ile) rs36087757 0.00003
NM_004360.5(CDH1):c.1477G>C (p.Val493Leu) rs730881666 0.00003
NM_004360.5(CDH1):c.1684A>T (p.Thr562Ser) rs587782061 0.00003
NM_004360.5(CDH1):c.2017C>A (p.Gln673Lys) rs587781701 0.00003
NM_004360.5(CDH1):c.1679C>T (p.Thr560Met) rs746481984 0.00002
NM_004360.5(CDH1):c.1946C>T (p.Ser649Phe) rs1238607560 0.00002
NM_004360.5(CDH1):c.2202A>T (p.Arg734Ser) rs745717070 0.00002
NM_004360.5(CDH1):c.2254G>A (p.Val752Ile) rs587781351 0.00002
NM_004360.5(CDH1):c.2359G>A (p.Val787Ile) rs766270336 0.00002
NM_004360.5(CDH1):c.2371C>T (p.Leu791Phe) rs786202598 0.00002
NM_004360.5(CDH1):c.2590G>A (p.Glu864Lys) rs142927667 0.00002
NM_004360.5(CDH1):c.2595G>C (p.Trp865Cys) rs778019174 0.00002
NM_004360.5(CDH1):c.2600A>G (p.Asn867Ser) rs587782623 0.00002
NM_004360.5(CDH1):c.325A>C (p.Lys109Gln) rs587782023 0.00002
NM_004360.5(CDH1):c.344C>T (p.Thr115Met) rs370973869 0.00002
NM_004360.5(CDH1):c.1070C>A (p.Thr357Lys) rs1260033180 0.00001
NM_004360.5(CDH1):c.1079C>G (p.Thr360Arg) rs549579183 0.00001
NM_004360.5(CDH1):c.112A>G (p.Thr38Ala) rs786203442 0.00001
NM_004360.5(CDH1):c.1171G>A (p.Val391Ile) rs556110297 0.00001
NM_004360.5(CDH1):c.1202C>A (p.Ala401Asp) rs150795245 0.00001
NM_004360.5(CDH1):c.1250A>G (p.Asn417Ser) rs773441320 0.00001
NM_004360.5(CDH1):c.125C>T (p.Pro42Leu) rs876659333 0.00001
NM_004360.5(CDH1):c.1315G>A (p.Ala439Thr) rs758764445 0.00001
NM_004360.5(CDH1):c.1334A>C (p.Glu445Ala) rs374398608 0.00001
NM_004360.5(CDH1):c.1351A>C (p.Ile451Leu) rs377416092 0.00001
NM_004360.5(CDH1):c.1370C>T (p.Thr457Met) rs587778170 0.00001
NM_004360.5(CDH1):c.1525A>G (p.Thr509Ala) rs761356661 0.00001
NM_004360.5(CDH1):c.1526C>A (p.Thr509Asn) rs771551231 0.00001
NM_004360.5(CDH1):c.1612G>T (p.Asp538Tyr) rs756154596 0.00001
NM_004360.5(CDH1):c.1633C>T (p.Arg545Trp) rs863224727 0.00001
NM_004360.5(CDH1):c.1843A>G (p.Ile615Val) rs1003012321 0.00001
NM_004360.5(CDH1):c.199G>A (p.Ala67Thr) rs1060501247 0.00001
NM_004360.5(CDH1):c.2026G>A (p.Asp676Asn) rs115408226 0.00001
NM_004360.5(CDH1):c.203A>G (p.Tyr68Cys) rs1284989530 0.00001
NM_004360.5(CDH1):c.2194C>T (p.Arg732Trp) rs864622198 0.00001
NM_004360.5(CDH1):c.2195G>T (p.Arg732Leu) rs1060501244 0.00001
NM_004360.5(CDH1):c.2201G>C (p.Arg734Thr) rs587781859 0.00001
NM_004360.5(CDH1):c.2281G>A (p.Gly761Arg) rs779648243 0.00001
NM_004360.5(CDH1):c.2318A>G (p.His773Arg) rs587782823 0.00001
NM_004360.5(CDH1):c.2398C>T (p.Arg800Cys) rs587782162 0.00001
NM_004360.5(CDH1):c.244G>A (p.Val82Met) rs1064793867 0.00001
NM_004360.5(CDH1):c.2459C>T (p.Thr820Ile) rs767159815 0.00001
NM_004360.5(CDH1):c.251C>T (p.Thr84Ile) rs754388534 0.00001
NM_004360.5(CDH1):c.2545A>G (p.Asn849Asp) rs876660881 0.00001
NM_004360.5(CDH1):c.2549C>G (p.Ser850Cys) rs1337211551 0.00001
NM_004360.5(CDH1):c.2602C>A (p.Arg868Ser) rs864622630 0.00001
NM_004360.5(CDH1):c.261G>C (p.Arg87Ser) rs878854689 0.00001
NM_004360.5(CDH1):c.2629G>A (p.Gly877Arg) rs555842031 0.00001
NM_004360.5(CDH1):c.387+1G>A rs587781919 0.00001
NM_004360.5(CDH1):c.602C>G (p.Pro201Arg) rs146777134 0.00001
NM_004360.5(CDH1):c.620T>C (p.Ile207Thr) rs778570149 0.00001
NM_004360.5(CDH1):c.631A>G (p.Thr211Ala) rs587781766 0.00001
NM_004360.5(CDH1):c.679A>G (p.Thr227Ala) rs1064796018 0.00001
NM_004360.5(CDH1):c.731A>G (p.Asp244Gly) rs1064794231 0.00001
NM_004360.5(CDH1):c.805G>A (p.Gly269Arg) rs750979600 0.00001
NM_004360.5(CDH1):c.901G>A (p.Ala301Thr) rs749056300 0.00001
NM_004360.5(CDH1):c.1003C>G (p.Arg335Gly) rs587780784
NM_004360.5(CDH1):c.1008+4A>G
NM_004360.5(CDH1):c.1024A>G (p.Thr342Ala)
NM_004360.5(CDH1):c.1073C>G (p.Thr358Arg) rs1191901557
NM_004360.5(CDH1):c.107G>A (p.Ser36Asn) rs1064794682
NM_004360.5(CDH1):c.1096A>G (p.Thr366Ala) rs1060501238
NM_004360.5(CDH1):c.1097C>G (p.Thr366Ser) rs876660260
NM_004360.5(CDH1):c.1103C>G (p.Thr368Ser) rs367868307
NM_004360.5(CDH1):c.1106A>G (p.Asn369Ser) rs1960858920
NM_004360.5(CDH1):c.1112A>G (p.Asn371Ser) rs1555515754
NM_004360.5(CDH1):c.112A>C (p.Thr38Pro) rs786203442
NM_004360.5(CDH1):c.1158G>T (p.Glu386Asp) rs2152133333
NM_004360.5(CDH1):c.1169A>G (p.Asn390Ser) rs964044070
NM_004360.5(CDH1):c.1183A>G (p.Thr395Ala) rs201135424
NM_004360.5(CDH1):c.1192G>A (p.Val398Met) rs2152133395
NM_004360.5(CDH1):c.1202C>T (p.Ala401Val) rs150795245
NM_004360.5(CDH1):c.1234G>A (p.Val412Ile) rs587782189
NM_004360.5(CDH1):c.1257TGG[1] (p.Gly421del) rs775730054
NM_004360.5(CDH1):c.1303A>G (p.Ile435Val) rs864622644
NM_004360.5(CDH1):c.1489G>A (p.Glu497Lys) rs1567508990
NM_004360.5(CDH1):c.1492G>A (p.Asp498Asn) rs2152135021
NM_004360.5(CDH1):c.149G>T (p.Arg50Leu)
NM_004360.5(CDH1):c.1538C>G (p.Pro513Arg)
NM_004360.5(CDH1):c.1550T>A (p.Met517Lys) rs786203656
NM_004360.5(CDH1):c.1570C>T (p.Arg524Trp) rs373605261
NM_004360.5(CDH1):c.1634G>A (p.Arg545Gln) rs587780115
NM_004360.5(CDH1):c.1675A>C (p.Ser559Arg)
NM_004360.5(CDH1):c.1676G>A (p.Ser559Asn) rs1596960625
NM_004360.5(CDH1):c.1693A>G (p.Ile565Val) rs1961080115
NM_004360.5(CDH1):c.1700C>T (p.Ala567Val) rs886041160
NM_004360.5(CDH1):c.1707C>A (p.Asp569Glu) rs876660905
NM_004360.5(CDH1):c.1711+2_1711+5dup
NM_004360.5(CDH1):c.1741C>T (p.Leu581Phe) rs1567512154
NM_004360.5(CDH1):c.1745T>G (p.Leu582Arg)
NM_004360.5(CDH1):c.1766A>G (p.Asn589Ser) rs1367108095
NM_004360.5(CDH1):c.1772A>G (p.Asn591Ser) rs1555516835
NM_004360.5(CDH1):c.1774G>T (p.Ala592Ser) rs35187787
NM_004360.5(CDH1):c.1789C>A (p.Pro597Thr) rs201625049
NM_004360.5(CDH1):c.178T>C (p.Cys60Arg)
NM_004360.5(CDH1):c.1819C>T (p.Pro607Ser)
NM_004360.5(CDH1):c.1832T>A (p.Val611Asp) rs779351070
NM_004360.5(CDH1):c.1864A>T (p.Asn622Tyr) rs367849039
NM_004360.5(CDH1):c.1868C>T (p.Thr623Ile) rs1961165592
NM_004360.5(CDH1):c.1960C>A (p.Pro654Thr) rs2152139271
NM_004360.5(CDH1):c.1979T>A (p.Val660Glu) rs1555517090
NM_004360.5(CDH1):c.200C>G (p.Ala67Gly) rs730881660
NM_004360.5(CDH1):c.202T>G (p.Tyr68Asp) rs1060501218
NM_004360.5(CDH1):c.2038A>C (p.Thr680Pro)
NM_004360.5(CDH1):c.2047G>A (p.Val683Ile)
NM_004360.5(CDH1):c.2080G>A (p.Val694Ile) rs587780118
NM_004360.5(CDH1):c.2135G>C (p.Gly712Ala)
NM_004360.5(CDH1):c.2152C>G (p.Leu718Val) rs876658591
NM_004360.5(CDH1):c.2165T>C (p.Ile722Thr) rs878854682
NM_004360.5(CDH1):c.2243C>A (p.Thr748Asn) rs1555517660
NM_004360.5(CDH1):c.2284G>A (p.Glu762Lys)
NM_004360.5(CDH1):c.2292C>A (p.Asp764Glu) rs61747636
NM_004360.5(CDH1):c.2296-17A>G rs2152142185
NM_004360.5(CDH1):c.2323G>A (p.Gly775Ser) rs1163417116
NM_004360.5(CDH1):c.2331C>G (p.Asp777Glu) rs114265540
NM_004360.5(CDH1):c.2356G>A (p.Asp786Asn) rs876659218
NM_004360.5(CDH1):c.2369C>A (p.Thr790Asn) rs587780120
NM_004360.5(CDH1):c.236C>G (p.Thr79Arg) rs876658359
NM_004360.5(CDH1):c.2396C>G (p.Pro799Arg) rs587781335
NM_004360.5(CDH1):c.2399G>T (p.Arg800Leu) rs370345996
NM_004360.5(CDH1):c.2401C>G (p.Pro801Ala) rs876660704
NM_004360.5(CDH1):c.2423G>A (p.Gly808Glu)
NM_004360.5(CDH1):c.2435A>G (p.Asp812Gly) rs878854684
NM_004360.5(CDH1):c.2467A>G (p.Thr823Ala) rs878854686
NM_004360.5(CDH1):c.2468C>T (p.Thr823Ile) rs1961533891
NM_004360.5(CDH1):c.2519C>T (p.Ser840Phe) rs587781300
NM_004360.5(CDH1):c.2574C>G (p.Asp858Glu) rs1060501245
NM_004360.5(CDH1):c.2593T>C (p.Trp865Arg) rs1555518267
NM_004360.5(CDH1):c.2624T>G (p.Met875Arg) rs900118000
NM_004360.5(CDH1):c.2647T>C (p.Ter883Gln) rs932491569
NM_004360.5(CDH1):c.304G>T (p.Ala102Ser) rs368492235
NM_004360.5(CDH1):c.313T>A (p.Ser105Thr) rs1165815510
NM_004360.5(CDH1):c.38T>C (p.Leu13Pro)
NM_004360.5(CDH1):c.458A>G (p.Lys153Arg)
NM_004360.5(CDH1):c.49-3C>A rs587782366
NM_004360.5(CDH1):c.524_525delinsAT (p.Leu175His)
NM_004360.5(CDH1):c.61C>T (p.Leu21Phe) rs863224729
NM_004360.5(CDH1):c.700G>A (p.Ala234Thr) rs878854694
NM_004360.5(CDH1):c.847G>C (p.Glu283Gln)
NM_004360.5(CDH1):c.865G>A (p.Ala289Thr) rs1255556757
NM_004360.5(CDH1):c.970G>A (p.Gly324Arg)
NM_004360.5(CDH1):c.995G>T (p.Gly332Val) rs1597894308

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