List of variants in gene AXIN2 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_004655.4(AXIN2):c.1386C>T (p.Pro462=)	rs1133683	0.52439
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.2282C>A (p.Ala761Asp)	rs79732150	0.00649
NM_004655.4(AXIN2):c.1070G>A (p.Arg357His)	rs8081536	0.00172
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.2051C>T (p.Ala684Val)	rs138287857	0.00112
NM_004655.4(AXIN2):c.1975C>T (p.Arg659Trp)	rs142670753	0.00014
NM_004655.4(AXIN2):c.2406-8C>G	rs143905290	0.00009
NM_004655.4(AXIN2):c.2182G>A (p.Ala728Thr)	rs141260153	0.00007
NM_004655.4(AXIN2):c.1222G>A (p.Glu408Lys)	rs749846538	0.00004
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.955G>A (p.Val319Ile)	rs913060347	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.1478C>G (p.Ser493Trp)	rs367697282	0.00003
NM_004655.4(AXIN2):c.1904A>G (p.His635Arg)	rs775207779	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.-116-13del	rs530658215
NM_004655.4(AXIN2):c.118G>A (p.Val40Met)	rs1555583743
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser)	rs115931022
NM_004655.4(AXIN2):c.1744A>G (p.Asn582Asp)	rs567511335

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