ClinVar Miner

List of variants in gene CTNNA3 reported as benign for arrhythmogenic right ventricular dysplasia 13

Included ClinVar conditions (1):
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Total variants: 26
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HGVS dbSNP
NM_013266.4(CTNNA3):c.1047C>T (p.Asn349=) rs60262757
NM_013266.4(CTNNA3):c.1133G>A (p.Arg378His) rs143682596
NM_013266.4(CTNNA3):c.1195C>A (p.Leu399Ile) rs115276158
NM_013266.4(CTNNA3):c.1215T>C (p.Asn405=) rs775938724
NM_013266.4(CTNNA3):c.156G>C (p.Ser52=) rs61759502
NM_013266.4(CTNNA3):c.1587_1588delinsAT (p.Asp529_Ala530delinsGluSer) rs1554949356
NM_013266.4(CTNNA3):c.1603C>T (p.Arg535Cys) rs41274090
NM_013266.4(CTNNA3):c.1611G>A (p.Ala537=) rs146900023
NM_013266.4(CTNNA3):c.1655C>T (p.Thr552Met) rs61737718
NM_013266.4(CTNNA3):c.1872C>A (p.Val624=) rs10997034
NM_013266.4(CTNNA3):c.1929C>T (p.His643=) rs147760277
NM_013266.4(CTNNA3):c.1959C>T (p.Thr653=) rs556623128
NM_013266.4(CTNNA3):c.2142G>A (p.Glu714=) rs115972723
NM_013266.4(CTNNA3):c.2158A>C (p.Arg720=) rs143867269
NM_013266.4(CTNNA3):c.2172A>C (p.Pro724=) rs116662854
NM_013266.4(CTNNA3):c.2553G>A (p.Lys851=) rs115814032
NM_013266.4(CTNNA3):c.33C>T (p.Ile11=) rs61735044
NM_013266.4(CTNNA3):c.348A>C (p.Pro116=) rs61749224
NM_013266.4(CTNNA3):c.393G>A (p.Ala131=) rs80182543
NM_013266.4(CTNNA3):c.399G>A (p.Thr133=) rs150376558
NM_013266.4(CTNNA3):c.429T>C (p.Asp143=) rs111880127
NM_013266.4(CTNNA3):c.478T>A (p.Ser160Thr) rs61749223
NM_013266.4(CTNNA3):c.483C>T (p.Leu161=) rs74142830
NM_013266.4(CTNNA3):c.580-8C>T rs141983252
NM_013266.4(CTNNA3):c.742G>T (p.Ala248Ser) rs192093851
NM_013266.4(CTNNA3):c.779A>G (p.Gln260Arg) rs190073606

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