List of variants in gene CTNNA1 reported as pathogenic for Hereditary diffuse gastric adenocarcinoma

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 54

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.385C>T (p.Arg129Ter)	rs758599826	0.00001
NM_001903.5(CTNNA1):c.1006del (p.Glu336fs)	rs2532447844
NM_001903.5(CTNNA1):c.1046C>A (p.Ser349Ter)	rs201056930
NM_001903.5(CTNNA1):c.1053C>A (p.Tyr351Ter)	rs1304131217
NM_001903.5(CTNNA1):c.1075G>T (p.Glu359Ter)	rs2532980348
NM_001903.5(CTNNA1):c.1078_1081del (p.Arg360fs)	rs1753991365
NM_001903.5(CTNNA1):c.1134dup (p.Arg379fs)	rs2532982253
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)	rs2533352646
NM_001903.5(CTNNA1):c.1330dup (p.Glu444fs)	rs1758714268
NM_001903.5(CTNNA1):c.1350del (p.Arg451fs)
NM_001903.5(CTNNA1):c.1351C>T (p.Arg451Ter)	rs201498915
NM_001903.5(CTNNA1):c.1430_1433del (p.Ser477fs)	rs2533588489
NM_001903.5(CTNNA1):c.1450dup (p.Met484fs)	rs2533589177
NM_001903.5(CTNNA1):c.1464dup (p.Glu489fs)	rs2533589473
NM_001903.5(CTNNA1):c.1473G>A (p.Trp491Ter)	rs2533589742
NM_001903.5(CTNNA1):c.1474dup (p.Glu492fs)	rs2533589704
NM_001903.5(CTNNA1):c.1480C>T (p.Gln494Ter)	rs1356240181
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)	rs2532178251
NM_001903.5(CTNNA1):c.1581dup (p.Ile528fs)	rs2150288001
NM_001903.5(CTNNA1):c.1598dup (p.Asp534fs)
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)	rs2533710424
NM_001903.5(CTNNA1):c.1768C>T (p.Gln590Ter)	rs926691029
NM_001903.5(CTNNA1):c.1815del (p.Met606fs)	rs2533734361
NM_001903.5(CTNNA1):c.1822G>T (p.Glu608Ter)	rs2150295101
NM_001903.5(CTNNA1):c.1904_1905del (p.Pro635fs)	rs2533819466
NM_001903.5(CTNNA1):c.1906del (p.Glu636fs)	rs2533819573
NM_001903.5(CTNNA1):c.1928_1929del (p.Asp642_Phe643insTer)	rs2533820112
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)	rs2532178816
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)	rs2532330256
NM_001903.5(CTNNA1):c.39G>A (p.Trp13Ter)	rs2532170453
NM_001903.5(CTNNA1):c.406dup (p.Thr136fs)	rs1581105774
NM_001903.5(CTNNA1):c.580del (p.Arg194fs)	rs2532349572
NM_001903.5(CTNNA1):c.583C>T (p.Gln195Ter)	rs1581119680
NM_001903.5(CTNNA1):c.608_623del (p.His203fs)	rs2532423112
NM_001903.5(CTNNA1):c.660_666del (p.Tyr222fs)	rs2532424023
NM_001903.5(CTNNA1):c.68dup (p.Ala24fs)	rs2149651992
NM_001903.5(CTNNA1):c.739C>T (p.Gln247Ter)	rs2149776199
NM_001903.5(CTNNA1):c.86del (p.Leu29fs)	rs745411817
NM_001903.5(CTNNA1):c.887dup (p.Ser297fs)	rs2532446276
NM_001903.5(CTNNA1):c.892G>T (p.Glu298Ter)	rs1581178228
NM_001903.5(CTNNA1):c.919del (p.Glu307fs)	rs1760848495
NM_001903.5(CTNNA1):c.994C>T (p.Arg332Ter)	rs371052704
NM_001903.5(CTNNA1):c.99del (p.Thr34fs)	rs2532171064

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