ClinVar Miner

List of variants in gene AXIN2 reported as benign for Hereditary cancer-predisposing syndrome

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.1365A>G (p.Pro455=) rs9915936 0.90382
NM_004655.4(AXIN2):c.1386C>T (p.Pro462=) rs1133683 0.52439
NM_004655.4(AXIN2):c.148C>T (p.Pro50Ser) rs2240308 0.39067
NM_004655.4(AXIN2):c.2062C>T (p.Leu688=) rs35415678 0.11118
NM_004655.4(AXIN2):c.432T>C (p.Ile144=) rs2240307 0.04207
NM_004655.4(AXIN2):c.1383C>T (p.Ser461=) rs9914661 0.01367
NM_004655.4(AXIN2):c.1615G>A (p.Val539Met) rs9913621 0.01361
NM_004655.4(AXIN2):c.1573C>G (p.Pro525Ala) rs73346297 0.00930
NM_004655.4(AXIN2):c.2282C>A (p.Ala761Asp) rs79732150 0.00649
NM_004655.4(AXIN2):c.2109G>A (p.Arg703=) rs116525755 0.00396
NM_004655.4(AXIN2):c.1410C>T (p.His470=) rs149483825 0.00394
NM_004655.4(AXIN2):c.1530G>A (p.Thr510=) rs141014640 0.00299
NM_004655.4(AXIN2):c.2439C>T (p.Ala813=) rs149533605 0.00157
NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro) rs145353986 0.00128
NM_004655.4(AXIN2):c.1952C>T (p.Ser651Leu) rs74006838 0.00128
NM_004655.4(AXIN2):c.1101C>T (p.Pro367=) rs141697521 0.00094
NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro) rs142476324 0.00084
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.2285G>A (p.Ser762Asn) rs117688560 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.2213C>T (p.Ser738Phe) rs139209450 0.00031
NM_004655.4(AXIN2):c.1059+8C>T rs367595502 0.00025
NM_004655.4(AXIN2):c.1637G>T (p.Gly546Val) rs145717795 0.00024
NM_004655.4(AXIN2):c.1829G>A (p.Arg610Gln) rs376248072 0.00018
NM_004655.4(AXIN2):c.1242G>A (p.Arg414=) rs200325634 0.00016
NM_004655.4(AXIN2):c.1305G>A (p.Pro435=) rs369221405 0.00014
NM_004655.4(AXIN2):c.1327C>T (p.Leu443=) rs371691797 0.00013
NM_004655.4(AXIN2):c.435C>A (p.Val145=) rs111470596 0.00013
NM_004655.4(AXIN2):c.1181G>A (p.Arg394His) rs200899695 0.00010
NM_004655.4(AXIN2):c.2406-8C>G rs143905290 0.00009
NM_004655.4(AXIN2):c.1623C>T (p.Cys541=) rs199931425 0.00008
NM_004655.4(AXIN2):c.738C>T (p.Thr246=) rs201191083 0.00008
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe) rs376630432 0.00006
NM_004655.4(AXIN2):c.2237+3G>A rs376584101 0.00006
NM_004655.4(AXIN2):c.522G>T (p.Ala174=) rs780914406 0.00002
NM_004655.4(AXIN2):c.1251G>T (p.Ala417=) rs557397475 0.00001
NM_004655.4(AXIN2):c.1802G>C (p.Gly601Ala) rs764140840 0.00001
NM_004655.4(AXIN2):c.1962C>A (p.Gly654=) rs377642903 0.00001
NM_004655.4(AXIN2):c.815+4A>G rs565020131 0.00001
NM_004655.4(AXIN2):c.-116-13del rs530658215
NM_004655.4(AXIN2):c.1200+18_1200+19delinsGC rs730881403
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser) rs115931022
NM_004655.4(AXIN2):c.1380T>C (p.Tyr460=) rs566313620
NM_004655.4(AXIN2):c.1404CCA[5] (p.His474del) rs570443161
NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup) rs570443161
NM_004655.4(AXIN2):c.2013_2024del (p.Thr672_Arg675del) rs151279728
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.435C>G (p.Val145=) rs111470596

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