ClinVar Miner

List of variants in gene EVC reported as benign for not provided

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Total variants: 38
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HGVS dbSNP
GRCh37/hg19 4p16.2(chr4:5731518-5778783)x1
NM_153717.3(EVC):c.1098+123A>G
NM_153717.3(EVC):c.1099-167G>C
NM_153717.3(EVC):c.1099-208C>A
NM_153717.3(EVC):c.1099-208C>T
NM_153717.3(EVC):c.1115C>T (p.Thr372Met) rs28483498
NM_153717.3(EVC):c.1315+271C>T
NM_153717.3(EVC):c.1316-139G>C
NM_153717.3(EVC):c.1316-220G>A
NM_153717.3(EVC):c.1464+177T>A
NM_153717.3(EVC):c.1464+236G>T
NM_153717.3(EVC):c.1465-285A>G
NM_153717.3(EVC):c.1563+185A>G
NM_153717.3(EVC):c.174+238T>A
NM_153717.3(EVC):c.1776+206C>G
NM_153717.3(EVC):c.1855G>A (p.Val619Ile) rs111293777
NM_153717.3(EVC):c.1886+172C>A
NM_153717.3(EVC):c.1886+202G>C
NM_153717.3(EVC):c.1886+253C>T
NM_153717.3(EVC):c.1886+266G>A
NM_153717.3(EVC):c.1887-122G>A
NM_153717.3(EVC):c.2097+111A>C
NM_153717.3(EVC):c.2449+317A>T
NM_153717.3(EVC):c.2561+144G>T
NM_153717.3(EVC):c.2561+221A>G
NM_153717.3(EVC):c.2782+103C>T
NM_153717.3(EVC):c.2782+145G>T
NM_153717.3(EVC):c.2782+173G>T
NM_153717.3(EVC):c.2894+248A>T
NM_153717.3(EVC):c.2895-114A>G
NM_153717.3(EVC):c.2895-249T>C
NM_153717.3(EVC):c.300+213C>T
NM_153717.3(EVC):c.301-80G>A
NM_153717.3(EVC):c.385-170T>A
NM_153717.3(EVC):c.769_772delinsTTAC (p.Tyr258His) rs1553871815
NM_153717.3(EVC):c.780G>A (p.Lys260=) rs41269555
NM_153717.3(EVC):c.802-311T>C
NM_153717.3(EVC):c.939+224C>T

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