ClinVar Miner

List of variants in gene AXIN2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.1530G>A (p.Thr510=) rs141014640 0.00299
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val) rs138287857 0.00112
NM_004655.4(AXIN2):c.1101C>T (p.Pro367=) rs141697521 0.00094
NM_004655.4(AXIN2):c.270C>T (p.Asp90=) rs141655687 0.00076
NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly) rs139871607 0.00075
NM_004655.4(AXIN2):c.1545C>T (p.His515=) rs139316692 0.00070
NM_004655.4(AXIN2):c.1250C>T (p.Ala417Val) rs201460658 0.00064
NM_004655.4(AXIN2):c.2052G>A (p.Ala684=) rs200573256 0.00046
NM_004655.4(AXIN2):c.733C>T (p.Pro245Ser) rs62640028 0.00043
NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu) rs149764887 0.00031
NM_004655.4(AXIN2):c.1305G>A (p.Pro435=) rs369221405 0.00014
NM_004655.4(AXIN2):c.2004G>A (p.Gly668=) rs144092307 0.00004
NM_004655.4(AXIN2):c.1976G>A (p.Arg659Gln) rs730881400 0.00002
NM_004655.4(AXIN2):c.2262A>C (p.Ala754=) rs1060504485 0.00001
NM_004655.4(AXIN2):c.2271C>T (p.His757=) rs772041910 0.00001
NM_004655.4(AXIN2):c.*476_*487del
NM_004655.4(AXIN2):c.1095G>A (p.Val365=) rs754059595
NM_004655.4(AXIN2):c.1500C>A (p.Leu500=) rs745903369
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=) rs143243661

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