ClinVar Miner

List of variants in gene CTNNA1 studied for Hereditary diffuse gastric adenocarcinoma

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_001903.5(CTNNA1):c.2493G>C (p.Gln831His) rs781450977 0.00005
NM_001903.5(CTNNA1):c.385C>T (p.Arg129Ter) rs758599826 0.00001
NM_001903.5(CTNNA1):c.611G>A (p.Arg204His) rs1025792545 0.00001
NM_001903.5(CTNNA1):c.1006del (p.Glu336fs)
NM_001903.5(CTNNA1):c.1046C>A (p.Ser349Ter)
NM_001903.5(CTNNA1):c.105+1G>C rs374313094
NM_001903.5(CTNNA1):c.1053C>A (p.Tyr351Ter)
NM_001903.5(CTNNA1):c.1075G>T (p.Glu359Ter)
NM_001903.5(CTNNA1):c.1078_1081del (p.Arg360fs) rs1753991365
NM_001903.5(CTNNA1):c.1134dup (p.Arg379fs)
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.1350del (p.Arg451fs)
NM_001903.5(CTNNA1):c.1351C>T (p.Arg451Ter) rs201498915
NM_001903.5(CTNNA1):c.1390-6_1392delinsA
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.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)
NM_001903.5(CTNNA1):c.1768C>T (p.Gln590Ter) rs926691029
NM_001903.5(CTNNA1):c.1815del (p.Met606fs)
NM_001903.5(CTNNA1):c.1822G>T (p.Glu608Ter)
NM_001903.5(CTNNA1):c.1899+1G>C rs1580862601
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.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.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.468+1G>T
NM_001903.5(CTNNA1):c.580del (p.Arg194fs)
NM_001903.5(CTNNA1):c.583C>T (p.Gln195Ter)
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.887dup (p.Ser297fs)
NM_001903.5(CTNNA1):c.892G>T (p.Glu298Ter)
NM_001903.5(CTNNA1):c.919del (p.Glu307fs) rs1760848495
NM_001903.5(CTNNA1):c.994C>T (p.Arg332Ter)
NM_001903.5(CTNNA1):c.99del (p.Thr34fs)

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