List of variants in gene AXIN2 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 49

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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.*1012T>A	rs7591	0.48929
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.*957T>G	rs112415132	0.03202
NM_004655.4(AXIN2):c.1383C>T (p.Ser461=)	rs9914661	0.01367
NM_004655.4(AXIN2):c.*846G>A	rs75257056	0.01027
NM_004655.4(AXIN2):c.*309C>A	rs192185171	0.00463
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.1807G>C (p.Ala603Pro)	rs145353986	0.00128
NM_004655.4(AXIN2):c.1532C>T (p.Thr511Met)	rs200883019	0.00109
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.*147C>T	rs150336911	0.00076
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.*500T>G	rs187274855	0.00073
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.1685C>T (p.Pro562Leu)	rs149764887	0.00031
NM_004655.4(AXIN2):c.1059+8C>T	rs367595502	0.00025
NM_004655.4(AXIN2):c.-33A>C	rs190687283	0.00024
NM_004655.4(AXIN2):c.1242G>A (p.Arg414=)	rs200325634	0.00016
NM_004655.4(AXIN2):c.780T>C (p.Ser260=)	rs147681058	0.00016
NM_004655.4(AXIN2):c.1327C>T (p.Leu443=)	rs371691797	0.00013
NM_004655.4(AXIN2):c.144C>T (p.Pro48=)	rs144099816	0.00013
NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp)	rs200201811	0.00011
NM_004655.4(AXIN2):c.1376G>A (p.Arg459His)	rs368525111	0.00010
NM_004655.4(AXIN2):c.2406-8C>G	rs143905290	0.00009
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe)	rs376630432	0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val)	rs201531372	0.00006
NM_004655.4(AXIN2):c.*326A>G	rs533959126	0.00004
NM_004655.4(AXIN2):c.2004G>A (p.Gly668=)	rs144092307	0.00004
NM_004655.4(AXIN2):c.645C>T (p.Leu215=)	rs767834824	0.00003
NM_004655.4(AXIN2):c.1887G>A (p.Gln629=)	rs140163819	0.00002
NM_004655.4(AXIN2):c.1200+8G>A	rs776372607	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.*794C>A	rs10438779
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser)	rs115931022
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=)	rs143243661
NM_004655.4(AXIN2):c.629T>C (p.Met210Thr)	rs529954883

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