ClinVar Miner

List of variants in gene AXIN2 reported as uncertain significance for colorectal carcinoma

Included ClinVar conditions (14):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.2182G>A (p.Ala728Thr) rs141260153 0.00007
NM_004655.4(AXIN2):c.1553A>G (p.Tyr518Cys) rs368289818 0.00004
NM_004655.4(AXIN2):c.2216A>G (p.Asn739Ser) rs547630327 0.00004
NM_004655.4(AXIN2):c.1093G>A (p.Val365Met) rs761901627 0.00003
NM_004655.4(AXIN2):c.1363C>G (p.Pro455Ala) rs779863826 0.00003
NM_004655.4(AXIN2):c.1651T>C (p.Cys551Arg) rs730881398 0.00001
NM_004655.4(AXIN2):c.1708T>G (p.Phe570Val) rs373442399 0.00001
NM_004655.4(AXIN2):c.2000G>A (p.Ser667Asn) rs878854724 0.00001
NM_004655.4(AXIN2):c.1744A>G (p.Asn582Asp) rs567511335

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