Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.218890262G>ACA350586994WNT10Ac.655G>A (p.Gly219Ser)
c.264-2512G>A
c.604G>A (p.Gly202Ser)
c.559G>A (p.Gly187Ser)
c.377-2512G>A (n.377-2512G>A)
2g.218890262G>CCA350586997WNT10Ac.655G>C (p.Gly219Arg)
c.264-2512G>C
c.604G>C (p.Gly202Arg)
c.559G>C (p.Gly187Arg)
c.377-2512G>C (n.377-2512G>C)
2g.218890262G>TCA350587004WNT10Ac.655G>T (p.Gly219Cys)
c.264-2512G>T
c.604G>T (p.Gly202Cys)
c.559G>T (p.Gly187Cys)
c.377-2512G>T (n.377-2512G>T)
2g.218890263G>ACA350587011WNT10Ac.656G>A (p.Gly219Asp)
c.264-2511G>A
c.605G>A (p.Gly202Asp)
c.560G>A (p.Gly187Asp)
c.377-2511G>A (n.377-2511G>A)
 dbSNP gnomAD v2 gnomAD v4
2g.218890263G>CCA350587014WNT10Ac.656G>C (p.Gly219Ala)
c.264-2511G>C
c.605G>C (p.Gly202Ala)
c.560G>C (p.Gly187Ala)
c.377-2511G>C (n.377-2511G>C)
2g.218890263G=CA1328965146WNT10Ac.656G= (p.Gly219=)
c.264-2511G=
c.605G= (p.Gly202=)
c.560G= (p.Gly187=)
c.377-2511G= (n.377-2511G=)
2g.218890263G>TCA350587015WNT10Ac.656G>T (p.Gly219Val)
c.264-2511G>T
c.605G>T (p.Gly202Val)
c.560G>T (p.Gly187Val)
c.377-2511G>T (n.377-2511G>T)
2g.218890264C>ACA431416799WNT10Ac.657C>A (p.Gly219=)
c.264-2510C>A
c.606C>A (p.Gly202=)
c.561C>A (p.Gly187=)
c.377-2510C>A (n.377-2510C>A)
 dbSNP gnomAD v2 COSMIC
2g.218890264C=CA1328965147WNT10Ac.657C= (p.Gly219=)
c.264-2510C=
c.606C= (p.Gly202=)
c.561C= (p.Gly187=)
c.377-2510C= (n.377-2510C=)
2g.218890264C>GCA431416800WNT10Ac.657C>G (p.Gly219=)
c.264-2510C>G
c.606C>G (p.Gly202=)
c.561C>G (p.Gly187=)
c.377-2510C>G (n.377-2510C>G)
2g.218890264C>TCA431416801WNT10Ac.657C>T (p.Gly219=)
c.264-2510C>T
c.606C>T (p.Gly202=)
c.561C>T (p.Gly187=)
c.377-2510C>T (n.377-2510C>T)
2g.218890265T>ACA350587017WNT10Ac.658T>A (p.Phe220Ile)
c.264-2509T>A
c.607T>A (p.Phe203Ile)
c.562T>A (p.Phe188Ile)
c.377-2509T>A (n.377-2509T>A)
2g.218890265T>CCA350587019WNT10Ac.658T>C (p.Phe220Leu)
c.264-2509T>C
c.607T>C (p.Phe203Leu)
c.562T>C (p.Phe188Leu)
c.377-2509T>C (n.377-2509T>C)
2g.218890265T>GCA350587022WNT10Ac.658T>G (p.Phe220Val)
c.264-2509T>G
c.607T>G (p.Phe203Val)
c.562T>G (p.Phe188Val)
c.377-2509T>G (n.377-2509T>G)
2g.218890268_218890281delCA2663174292WNT10Ac.661_674del (p.Gly221Ter)
c.264-2506_264-2493del
c.610_623del (p.Gly204Ter)
c.565_578del (p.Gly189Ter)
c.377-2506_377-2493del (n.377-2506_377-2493del)
 gnomAD v4
2g.218890266T>ACA350587027WNT10Ac.659T>A (p.Phe220Tyr)
c.264-2508T>A
c.608T>A (p.Phe203Tyr)
c.563T>A (p.Phe188Tyr)
c.377-2508T>A (n.377-2508T>A)
2g.218890266T>CCA350587030WNT10Ac.659T>C (p.Phe220Ser)
c.264-2508T>C
c.608T>C (p.Phe203Ser)
c.563T>C (p.Phe188Ser)
c.377-2508T>C (n.377-2508T>C)
 gnomAD v4
2g.218890266T>GCA350587035WNT10Ac.659T>G (p.Phe220Cys)
c.264-2508T>G
c.608T>G (p.Phe203Cys)
c.563T>G (p.Phe188Cys)
c.377-2508T>G (n.377-2508T>G)
2g.218890267C>ACA350587040WNT10Ac.660C>A (p.Phe220Leu)
c.264-2507C>A
c.609C>A (p.Phe203Leu)
c.564C>A (p.Phe188Leu)
c.377-2507C>A (n.377-2507C>A)
2g.218890267C=CA1328965150WNT10Ac.660C= (p.Phe220=)
c.264-2507C=
c.609C= (p.Phe203=)
c.564C= (p.Phe188=)
c.377-2507C= (n.377-2507C=)
2g.218890267C>GCA350587050WNT10Ac.660C>G (p.Phe220Leu)
c.264-2507C>G
c.609C>G (p.Phe203Leu)
c.564C>G (p.Phe188Leu)
c.377-2507C>G (n.377-2507C>G)
2g.218890267C>TCA2113989WNT10Ac.660C>T (p.Phe220=)
c.264-2507C>T
c.609C>T (p.Phe203=)
c.564C>T (p.Phe188=)
c.377-2507C>T (n.377-2507C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.218890268G>ACA2113990WNT10Ac.661G>A (p.Gly221Arg)
c.264-2506G>A
c.610G>A (p.Gly204Arg)
c.565G>A (p.Gly189Arg)
c.377-2506G>A (n.377-2506G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890268G>CCA350587051WNT10Ac.661G>C (p.Gly221Arg)
c.264-2506G>C
c.610G>C (p.Gly204Arg)
c.565G>C (p.Gly189Arg)
c.377-2506G>C (n.377-2506G>C)
2g.218890268G=CA1328965154WNT10Ac.661G= (p.Gly221=)
c.264-2506G=
c.610G= (p.Gly204=)
c.565G= (p.Gly189=)
c.377-2506G= (n.377-2506G=)
2g.218890268G>TCA350587052WNT10Ac.661G>T (p.Gly221Trp)
c.264-2506G>T
c.610G>T (p.Gly204Trp)
c.565G>T (p.Gly189Trp)
c.377-2506G>T (n.377-2506G>T)
2g.218890271delCA2663174293WNT10Ac.664del (p.Glu222SerfsTer21)
c.264-2503del
c.613del (p.Glu205SerfsTer21)
c.568del (p.Glu190SerfsTer21)
c.377-2503del (n.377-2503del)
 gnomAD v4
2g.218890269G>ACA350587055WNT10Ac.662G>A (p.Gly221Glu)
c.264-2505G>A
c.611G>A (p.Gly204Glu)
c.566G>A (p.Gly189Glu)
c.377-2505G>A (n.377-2505G>A)
2g.218890269G>CCA350587057WNT10Ac.662G>C (p.Gly221Ala)
c.264-2505G>C
c.611G>C (p.Gly204Ala)
c.566G>C (p.Gly189Ala)
c.377-2505G>C (n.377-2505G>C)
2g.218890269G=CA1328965157WNT10Ac.662G= (p.Gly221=)
c.264-2505G=
c.611G= (p.Gly204=)
c.566G= (p.Gly189=)
c.377-2505G= (n.377-2505G=)
2g.218890269G>TCA2113991WNT10Ac.662G>T (p.Gly221Val)
c.264-2505G>T
c.611G>T (p.Gly204Val)
c.566G>T (p.Gly189Val)
c.377-2505G>T (n.377-2505G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890270G>ACA431416812WNT10Ac.663G>A (p.Gly221=)
c.264-2504G>A
c.612G>A (p.Gly204=)
c.567G>A (p.Gly189=)
c.377-2504G>A (n.377-2504G>A)
 ClinVar gnomAD v4
2g.218890270G>CCA431416811WNT10Ac.663G>C (p.Gly221=)
c.264-2504G>C
c.612G>C (p.Gly204=)
c.567G>C (p.Gly189=)
c.377-2504G>C (n.377-2504G>C)
2g.218890270G>TCA431416810WNT10Ac.663G>T (p.Gly221=)
c.264-2504G>T
c.612G>T (p.Gly204=)
c.567G>T (p.Gly189=)
c.377-2504G>T (n.377-2504G>T)
 gnomAD v4
2g.218890271G>ACA350587059WNT10Ac.664G>A (p.Glu222Lys)
c.264-2503G>A
c.613G>A (p.Glu205Lys)
c.568G>A (p.Glu190Lys)
c.377-2503G>A (n.377-2503G>A)
 ClinVar dbSNP
2g.218890271G>CCA350587060WNT10Ac.664G>C (p.Glu222Gln)
c.264-2503G>C
c.613G>C (p.Glu205Gln)
c.568G>C (p.Glu190Gln)
c.377-2503G>C (n.377-2503G>C)
 dbSNP gnomAD v4 COSMIC
2g.218890271G=CA1328965160WNT10Ac.664G= (p.Glu222=)
c.264-2503G=
c.613G= (p.Glu205=)
c.568G= (p.Glu190=)
c.377-2503G= (n.377-2503G=)
2g.218890271G>TCA2113992WNT10Ac.664G>T (p.Glu222Ter)
c.264-2503G>T
c.613G>T (p.Glu205Ter)
c.568G>T (p.Glu190Ter)
c.377-2503G>T (n.377-2503G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890272A>CCA350587065WNT10Ac.665A>C (p.Glu222Ala)
c.264-2502A>C
c.614A>C (p.Glu205Ala)
c.569A>C (p.Glu190Ala)
c.377-2502A>C (n.377-2502A>C)
2g.218890272A>GCA350587067WNT10Ac.665A>G (p.Glu222Gly)
c.264-2502A>G
c.614A>G (p.Glu205Gly)
c.569A>G (p.Glu190Gly)
c.377-2502A>G (n.377-2502A>G)
2g.218890272A>TCA350587069WNT10Ac.665A>T (p.Glu222Val)
c.264-2502A>T
c.614A>T (p.Glu205Val)
c.569A>T (p.Glu190Val)
c.377-2502A>T (n.377-2502A>T)
2g.218890273G>ACA65916922WNT10Ac.666G>A (p.Glu222=)
c.264-2501G>A
c.615G>A (p.Glu205=)
c.570G>A (p.Glu190=)
c.377-2501G>A (n.377-2501G>A)
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.218890273G>CCA65916917WNT10Ac.666G>C (p.Glu222Asp)
c.264-2501G>C
c.615G>C (p.Glu205Asp)
c.570G>C (p.Glu190Asp)
c.377-2501G>C (n.377-2501G>C)
 dbSNP gnomAD v3 gnomAD v4
2g.218890273G=CA1328965164WNT10Ac.666G= (p.Glu222=)
c.264-2501G=
c.615G= (p.Glu205=)
c.570G= (p.Glu190=)
c.377-2501G= (n.377-2501G=)
2g.218890273G>TCA350587070WNT10Ac.666G>T (p.Glu222Asp)
c.264-2501G>T
c.615G>T (p.Glu205Asp)
c.570G>T (p.Glu190Asp)
c.377-2501G>T (n.377-2501G>T)
2g.218890274C>ACA2113994WNT10Ac.667C>A (p.Arg223Ser)
c.264-2500C>A
c.616C>A (p.Arg206Ser)
c.571C>A (p.Arg191Ser)
c.377-2500C>A (n.377-2500C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890274C=CA1328965167WNT10Ac.667C= (p.Arg223=)
c.264-2500C=
c.616C= (p.Arg206=)
c.571C= (p.Arg191=)
c.377-2500C= (n.377-2500C=)
2g.218890274C>GCA350587075WNT10Ac.667C>G (p.Arg223Gly)
c.264-2500C>G
c.616C>G (p.Arg206Gly)
c.571C>G (p.Arg191Gly)
c.377-2500C>G (n.377-2500C>G)
2g.218890274C>TCA2113993WNT10Ac.667C>T (p.Arg223Cys)
c.264-2500C>T
c.616C>T (p.Arg206Cys)
c.571C>T (p.Arg191Cys)
c.377-2500C>T (n.377-2500C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890275G>ACA2113995WNT10Ac.668G>A (p.Arg223His)
c.264-2499G>A
c.617G>A (p.Arg206His)
c.572G>A (p.Arg191His)
c.377-2499G>A (n.377-2499G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890275G>CCA350587080WNT10Ac.668G>C (p.Arg223Pro)
c.264-2499G>C
c.617G>C (p.Arg206Pro)
c.572G>C (p.Arg191Pro)
c.377-2499G>C (n.377-2499G>C)
2g.218890275G=CA1328965170WNT10Ac.668G= (p.Arg223=)
c.264-2499G=
c.617G= (p.Arg206=)
c.572G= (p.Arg191=)
c.377-2499G= (n.377-2499G=)
2g.218890275G>TCA350587083WNT10Ac.668G>T (p.Arg223Leu)
c.264-2499G>T
c.617G>T (p.Arg206Leu)
c.572G>T (p.Arg191Leu)
c.377-2499G>T (n.377-2499G>T)
 COSMIC
2g.218890275dupCA539840803WNT10Ac.668dup (p.Phe224LeufsTer3)
c.264-2499dup
c.617dup (p.Phe207LeufsTer3)
c.572dup (p.Phe192LeufsTer3)
c.377-2499dup (n.377-2499dup)
 dbSNP gnomAD v2 gnomAD v4
2g.218890276C>ACA431416821WNT10Ac.669C>A (p.Arg223=)
c.264-2498C>A
c.618C>A (p.Arg206=)
c.573C>A (p.Arg191=)
c.377-2498C>A (n.377-2498C>A)
2g.218890276C>GCA431416823WNT10Ac.669C>G (p.Arg223=)
c.264-2498C>G
c.618C>G (p.Arg206=)
c.573C>G (p.Arg191=)
c.377-2498C>G (n.377-2498C>G)
2g.218890276C>TCA431416822WNT10Ac.669C>T (p.Arg223=)
c.264-2498C>T
c.618C>T (p.Arg206=)
c.573C>T (p.Arg191=)
c.377-2498C>T (n.377-2498C>T)
2g.218890277T>ACA350587087WNT10Ac.670T>A (p.Phe224Ile)
c.264-2497T>A
c.619T>A (p.Phe207Ile)
c.574T>A (p.Phe192Ile)
c.377-2497T>A (n.377-2497T>A)
2g.218890277T>CCA2113996WNT10Ac.670T>C (p.Phe224Leu)
c.264-2497T>C
c.619T>C (p.Phe207Leu)
c.574T>C (p.Phe192Leu)
c.377-2497T>C (n.377-2497T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890277T>GCA350587090WNT10Ac.670T>G (p.Phe224Val)
c.264-2497T>G
c.619T>G (p.Phe207Val)
c.574T>G (p.Phe192Val)
c.377-2497T>G (n.377-2497T>G)
2g.218890277T=CA1328965174WNT10Ac.670T= (p.Phe224=)
c.264-2497T=
c.619T= (p.Phe207=)
c.574T= (p.Phe192=)
c.377-2497T= (n.377-2497T=)
2g.218890280delCA2580065722WNT10Ac.673del (p.Ser225LeufsTer18)
c.264-2494del
c.622del (p.Ser208LeufsTer18)
c.577del (p.Ser193LeufsTer18)
c.377-2494del (n.377-2494del)
 ClinVar
2g.218890278T>ACA350587093WNT10Ac.671T>A (p.Phe224Tyr)
c.264-2496T>A
c.620T>A (p.Phe207Tyr)
c.575T>A (p.Phe192Tyr)
c.377-2496T>A (n.377-2496T>A)
2g.218890278T>CCA350587095WNT10Ac.671T>C (p.Phe224Ser)
c.264-2496T>C
c.620T>C (p.Phe207Ser)
c.575T>C (p.Phe192Ser)
c.377-2496T>C (n.377-2496T>C)
 gnomAD v4
2g.218890278T>GCA350587098WNT10Ac.671T>G (p.Phe224Cys)
c.264-2496T>G
c.620T>G (p.Phe207Cys)
c.575T>G (p.Phe192Cys)
c.377-2496T>G (n.377-2496T>G)
2g.218890279T>ACA350587104WNT10Ac.672T>A (p.Phe224Leu)
c.264-2495T>A
c.621T>A (p.Phe207Leu)
c.576T>A (p.Phe192Leu)
c.377-2495T>A (n.377-2495T>A)
2g.218890279T>CCA431416830WNT10Ac.672T>C (p.Phe224=)
c.264-2495T>C
c.621T>C (p.Phe207=)
c.576T>C (p.Phe192=)
c.377-2495T>C (n.377-2495T>C)
 gnomAD v4
2g.218890279T>GCA350587101WNT10Ac.672T>G (p.Phe224Leu)
c.264-2495T>G
c.621T>G (p.Phe207Leu)
c.576T>G (p.Phe192Leu)
c.377-2495T>G (n.377-2495T>G)
2g.218890280T>ACA350587107WNT10Ac.673T>A (p.Ser225Thr)
c.264-2494T>A
c.622T>A (p.Ser208Thr)
c.577T>A (p.Ser193Thr)
c.377-2494T>A (n.377-2494T>A)
2g.218890280T>CCA350587112WNT10Ac.673T>C (p.Ser225Pro)
c.264-2494T>C
c.622T>C (p.Ser208Pro)
c.577T>C (p.Ser193Pro)
c.377-2494T>C (n.377-2494T>C)
2g.218890280T>GCA350587110WNT10Ac.673T>G (p.Ser225Ala)
c.264-2494T>G
c.622T>G (p.Ser208Ala)
c.577T>G (p.Ser193Ala)
c.377-2494T>G (n.377-2494T>G)
2g.218890281C>ACA350587117WNT10Ac.674C>A (p.Ser225Tyr)
c.264-2493C>A
c.623C>A (p.Ser208Tyr)
c.578C>A (p.Ser193Tyr)
c.377-2493C>A (n.377-2493C>A)
2g.218890281C>GCA350587128WNT10Ac.674C>G (p.Ser225Cys)
c.264-2493C>G
c.623C>G (p.Ser208Cys)
c.578C>G (p.Ser193Cys)
c.377-2493C>G (n.377-2493C>G)
2g.218890281C>TCA350587131WNT10Ac.674C>T (p.Ser225Phe)
c.264-2493C>T
c.623C>T (p.Ser208Phe)
c.578C>T (p.Ser193Phe)
c.377-2493C>T (n.377-2493C>T)
 gnomAD v4
2g.218890282T>ACA431416836WNT10Ac.675T>A (p.Ser225=)
c.264-2492T>A
c.624T>A (p.Ser208=)
c.579T>A (p.Ser193=)
c.377-2492T>A (n.377-2492T>A)
2g.218890282T>CCA431416838WNT10Ac.675T>C (p.Ser225=)
c.264-2492T>C
c.624T>C (p.Ser208=)
c.579T>C (p.Ser193=)
c.377-2492T>C (n.377-2492T>C)
 dbSNP gnomAD v2 gnomAD v4
2g.218890282T>GCA431416840WNT10Ac.675T>G (p.Ser225=)
c.264-2492T>G
c.624T>G (p.Ser208=)
c.579T>G (p.Ser193=)
c.377-2492T>G (n.377-2492T>G)
2g.218890282T=CA1328965177WNT10Ac.675T= (p.Ser225=)
c.264-2492T=
c.624T= (p.Ser208=)
c.579T= (p.Ser193=)
c.377-2492T= (n.377-2492T=)
2g.218890283A=CA1328965178WNT10Ac.676A= (p.Lys226=)
c.264-2491A=
c.625A= (p.Lys209=)
c.580A= (p.Lys194=)
c.377-2491A= (n.377-2491A=)
2g.218890283A>CCA350587134WNT10Ac.676A>C (p.Lys226Gln)
c.264-2491A>C
c.625A>C (p.Lys209Gln)
c.580A>C (p.Lys194Gln)
c.377-2491A>C (n.377-2491A>C)
2g.218890283A>GCA350587137WNT10Ac.676A>G (p.Lys226Glu)
c.264-2491A>G
c.625A>G (p.Lys209Glu)
c.580A>G (p.Lys194Glu)
c.377-2491A>G (n.377-2491A>G)
 dbSNP gnomAD v2
2g.218890283A>TCA350587141WNT10Ac.676A>T (p.Lys226Ter)
c.264-2491A>T
c.625A>T (p.Lys209Ter)
c.580A>T (p.Lys194Ter)
c.377-2491A>T (n.377-2491A>T)
2g.218890284A>CCA350587144WNT10Ac.677A>C (p.Lys226Thr)
c.264-2490A>C
c.626A>C (p.Lys209Thr)
c.581A>C (p.Lys194Thr)
c.377-2490A>C (n.377-2490A>C)
2g.218890284A>GCA350587146WNT10Ac.677A>G (p.Lys226Arg)
c.264-2490A>G
c.626A>G (p.Lys209Arg)
c.581A>G (p.Lys194Arg)
c.377-2490A>G (n.377-2490A>G)
2g.218890284A>TCA350587148WNT10Ac.677A>T (p.Lys226Met)
c.264-2490A>T
c.626A>T (p.Lys209Met)
c.581A>T (p.Lys194Met)
c.377-2490A>T (n.377-2490A>T)
2g.218890285G>ACA431416843WNT10Ac.678G>A (p.Lys226=)
c.264-2489G>A
c.627G>A (p.Lys209=)
c.582G>A (p.Lys194=)
c.377-2489G>A (n.377-2489G>A)
 dbSNP
2g.218890285G>CCA350587152WNT10Ac.678G>C (p.Lys226Asn)
c.264-2489G>C
c.627G>C (p.Lys209Asn)
c.582G>C (p.Lys194Asn)
c.377-2489G>C (n.377-2489G>C)
 gnomAD v4 COSMIC
2g.218890285G=CA1328965179WNT10Ac.678G= (p.Lys226=)
c.264-2489G=
c.627G= (p.Lys209=)
c.582G= (p.Lys194=)
c.377-2489G= (n.377-2489G=)
2g.218890285G>TCA350587155WNT10Ac.678G>T (p.Lys226Asn)
c.264-2489G>T
c.627G>T (p.Lys209Asn)
c.582G>T (p.Lys194Asn)
c.377-2489G>T (n.377-2489G>T)
 dbSNP gnomAD v2
2g.218890286G>ACA350587165WNT10Ac.679G>A (p.Asp227Asn)
c.264-2488G>A
c.628G>A (p.Asp210Asn)
c.583G>A (p.Asp195Asn)
c.377-2488G>A (n.377-2488G>A)
 gnomAD v4
2g.218890286G>CCA350587159WNT10Ac.679G>C (p.Asp227His)
c.264-2488G>C
c.628G>C (p.Asp210His)
c.583G>C (p.Asp195His)
c.377-2488G>C (n.377-2488G>C)
2g.218890286G>TCA350587163WNT10Ac.679G>T (p.Asp227Tyr)
c.264-2488G>T
c.628G>T (p.Asp210Tyr)
c.583G>T (p.Asp195Tyr)
c.377-2488G>T (n.377-2488G>T)
2g.218890287A>CCA350587170WNT10Ac.680A>C (p.Asp227Ala)
c.264-2487A>C
c.629A>C (p.Asp210Ala)
c.584A>C (p.Asp195Ala)
c.377-2487A>C (n.377-2487A>C)
2g.218890287A>GCA350587172WNT10Ac.680A>G (p.Asp227Gly)
c.264-2487A>G
c.629A>G (p.Asp210Gly)
c.584A>G (p.Asp195Gly)
c.377-2487A>G (n.377-2487A>G)
2g.218890287A>TCA350587174WNT10Ac.680A>T (p.Asp227Val)
c.264-2487A>T
c.629A>T (p.Asp210Val)
c.584A>T (p.Asp195Val)
c.377-2487A>T (n.377-2487A>T)
2g.218890288C>ACA350587197WNT10Ac.681C>A (p.Asp227Glu)
c.264-2486C>A
c.630C>A (p.Asp210Glu)
c.585C>A (p.Asp195Glu)
c.377-2486C>A (n.377-2486C>A)
2g.218890288C>GCA350587202WNT10Ac.681C>G (p.Asp227Glu)
c.264-2486C>G
c.630C>G (p.Asp210Glu)
c.585C>G (p.Asp195Glu)
c.377-2486C>G (n.377-2486C>G)
2g.218890288C>TCA431416847WNT10Ac.681C>T (p.Asp227=)
c.264-2486C>T
c.630C>T (p.Asp210=)
c.585C>T (p.Asp195=)
c.377-2486C>T (n.377-2486C>T)
 ClinVar dbSNP
2g.218890289T>ACA116867WNT10Ac.682T>A (p.Phe228Ile)
c.264-2485T>A
c.631T>A (p.Phe211Ile)
c.586T>A (p.Phe196Ile)
c.377-2485T>A (n.377-2485T>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890289T>CCA350587208WNT10Ac.682T>C (p.Phe228Leu)
c.264-2485T>C
c.631T>C (p.Phe211Leu)
c.586T>C (p.Phe196Leu)
c.377-2485T>C (n.377-2485T>C)
2g.218890289T>GCA350587211WNT10Ac.682T>G (p.Phe228Val)
c.264-2485T>G
c.631T>G (p.Phe211Val)
c.586T>G (p.Phe196Val)
c.377-2485T>G (n.377-2485T>G)
2g.218890289T=CA1328965180WNT10Ac.682T= (p.Phe228=)
c.264-2485T=
c.631T= (p.Phe211=)
c.586T= (p.Phe196=)
c.377-2485T= (n.377-2485T=)
2g.218890290T>ACA350587216WNT10Ac.683T>A (p.Phe228Tyr)
c.264-2484T>A
c.632T>A (p.Phe211Tyr)
c.587T>A (p.Phe196Tyr)
c.377-2484T>A (n.377-2484T>A)
2g.218890290T>CCA350587217WNT10Ac.683T>C (p.Phe228Ser)
c.264-2484T>C
c.632T>C (p.Phe211Ser)
c.587T>C (p.Phe196Ser)
c.377-2484T>C (n.377-2484T>C)
2g.218890290T>GCA350587218WNT10Ac.683T>G (p.Phe228Cys)
c.264-2484T>G
c.632T>G (p.Phe211Cys)
c.587T>G (p.Phe196Cys)
c.377-2484T>G (n.377-2484T>G)
2g.218890291T>ACA350587220WNT10Ac.684T>A (p.Phe228Leu)
c.264-2483T>A
c.633T>A (p.Phe211Leu)
c.588T>A (p.Phe196Leu)
c.377-2483T>A (n.377-2483T>A)
2g.218890291T>CCA431416853WNT10Ac.684T>C (p.Phe228=)
c.264-2483T>C
c.633T>C (p.Phe211=)
c.588T>C (p.Phe196=)
c.377-2483T>C (n.377-2483T>C)
 gnomAD v4
2g.218890291T>GCA350587219WNT10Ac.684T>G (p.Phe228Leu)
c.264-2483T>G
c.633T>G (p.Phe211Leu)
c.588T>G (p.Phe196Leu)
c.377-2483T>G (n.377-2483T>G)
 ClinVar
2g.218890292C>ACA350587225WNT10Ac.685C>A (p.Leu229Met)
c.264-2482C>A
c.634C>A (p.Leu212Met)
c.589C>A (p.Leu197Met)
c.377-2482C>A (n.377-2482C>A)
2g.218890292C>GCA350587227WNT10Ac.685C>G (p.Leu229Val)
c.264-2482C>G
c.634C>G (p.Leu212Val)
c.589C>G (p.Leu197Val)
c.377-2482C>G (n.377-2482C>G)
 COSMIC
2g.218890292C>TCA431416858WNT10Ac.685C>T (p.Leu229=)
c.264-2482C>T
c.634C>T (p.Leu212=)
c.589C>T (p.Leu197=)
c.377-2482C>T (n.377-2482C>T)
 gnomAD v4
2g.218890293T>ACA350587232WNT10Ac.686T>A (p.Leu229Gln)
c.264-2481T>A
c.635T>A (p.Leu212Gln)
c.590T>A (p.Leu197Gln)
c.377-2481T>A (n.377-2481T>A)
2g.218890293T>CCA350587233WNT10Ac.686T>C (p.Leu229Pro)
c.264-2481T>C
c.635T>C (p.Leu212Pro)
c.590T>C (p.Leu197Pro)
c.377-2481T>C (n.377-2481T>C)
2g.218890293T>GCA350587246WNT10Ac.686T>G (p.Leu229Arg)
c.264-2481T>G
c.635T>G (p.Leu212Arg)
c.590T>G (p.Leu197Arg)
c.377-2481T>G (n.377-2481T>G)
 dbSNP gnomAD v2 gnomAD v4
2g.218890293T=CA1328965182WNT10Ac.686T= (p.Leu229=)
c.264-2481T=
c.635T= (p.Leu212=)
c.590T= (p.Leu197=)
c.377-2481T= (n.377-2481T=)
2g.218890294G>ACA431416860WNT10Ac.687G>A (p.Leu229=)
c.264-2480G>A
c.636G>A (p.Leu212=)
c.591G>A (p.Leu197=)
c.377-2480G>A (n.377-2480G>A)
2g.218890294G>CCA431416861WNT10Ac.687G>C (p.Leu229=)
c.264-2480G>C
c.636G>C (p.Leu212=)
c.591G>C (p.Leu197=)
c.377-2480G>C (n.377-2480G>C)
2g.218890294G>TCA431416862WNT10Ac.687G>T (p.Leu229=)
c.264-2480G>T
c.636G>T (p.Leu212=)
c.591G>T (p.Leu197=)
c.377-2480G>T (n.377-2480G>T)
2g.218890295G>ACA350587251WNT10Ac.688G>A (p.Asp230Asn)
c.264-2479G>A
c.637G>A (p.Asp213Asn)
c.592G>A (p.Asp198Asn)
c.377-2479G>A (n.377-2479G>A)
2g.218890295G>CCA350587254WNT10Ac.688G>C (p.Asp230His)
c.264-2479G>C
c.637G>C (p.Asp213His)
c.592G>C (p.Asp198His)
c.377-2479G>C (n.377-2479G>C)
2g.218890295G>TCA350587259WNT10Ac.688G>T (p.Asp230Tyr)
c.264-2479G>T
c.637G>T (p.Asp213Tyr)
c.592G>T (p.Asp198Tyr)
c.377-2479G>T (n.377-2479G>T)
 gnomAD v4
2g.218890296A=CA1328965184WNT10Ac.689A= (p.Asp230=)
c.264-2478A=
c.638A= (p.Asp213=)
c.593A= (p.Asp198=)
c.377-2478A= (n.377-2478A=)
2g.218890296A>CCA350587260WNT10Ac.689A>C (p.Asp230Ala)
c.264-2478A>C
c.638A>C (p.Asp213Ala)
c.593A>C (p.Asp198Ala)
c.377-2478A>C (n.377-2478A>C)
2g.218890296A>GCA2113997WNT10Ac.689A>G (p.Asp230Gly)
c.264-2478A>G
c.638A>G (p.Asp213Gly)
c.593A>G (p.Asp198Gly)
c.377-2478A>G (n.377-2478A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890296A>TCA350587261WNT10Ac.689A>T (p.Asp230Val)
c.264-2478A>T
c.638A>T (p.Asp213Val)
c.593A>T (p.Asp198Val)
c.377-2478A>T (n.377-2478A>T)
2g.218890297C>ACA2113998WNT10Ac.690C>A (p.Asp230Glu)
c.264-2477C>A
c.639C>A (p.Asp213Glu)
c.594C>A (p.Asp198Glu)
c.377-2477C>A (n.377-2477C>A)
 dbSNP ExAC gnomAD v4
2g.218890297C=CA1328965186WNT10Ac.690C= (p.Asp230=)
c.264-2477C=
c.639C= (p.Asp213=)
c.594C= (p.Asp198=)
c.377-2477C= (n.377-2477C=)
2g.218890297C>GCA350587265WNT10Ac.690C>G (p.Asp230Glu)
c.264-2477C>G
c.639C>G (p.Asp213Glu)
c.594C>G (p.Asp198Glu)
c.377-2477C>G (n.377-2477C>G)
2g.218890297C>TCA431416865WNT10Ac.690C>T (p.Asp230=)
c.264-2477C>T
c.639C>T (p.Asp213=)
c.594C>T (p.Asp198=)
c.377-2477C>T (n.377-2477C>T)
 ClinVar dbSNP gnomAD v4
2g.218890298T>ACA350587274WNT10Ac.691T>A (p.Ser231Thr)
c.264-2476T>A
c.640T>A (p.Ser214Thr)
c.595T>A (p.Ser199Thr)
c.377-2476T>A (n.377-2476T>A)
2g.218890298T>CCA350587269WNT10Ac.691T>C (p.Ser231Pro)
c.264-2476T>C
c.640T>C (p.Ser214Pro)
c.595T>C (p.Ser199Pro)
c.377-2476T>C (n.377-2476T>C)
2g.218890298T>GCA350587271WNT10Ac.691T>G (p.Ser231Ala)
c.264-2476T>G
c.640T>G (p.Ser214Ala)
c.595T>G (p.Ser199Ala)
c.377-2476T>G (n.377-2476T>G)
2g.218890298_218890299delinsTCCA1328965188WNT10Ac.691_692delinsTC (p.Ser231=)
c.264-2476_264-2475delinsTC
c.640_641delinsTC (p.Ser214=)
c.595_596delinsTC (p.Ser199=)
c.377-2476_377-2475delinsTC (n.377-2476_377-2475delinsTC)
2g.218890299C>ACA350587279WNT10Ac.692C>A (p.Ser231Tyr)
c.264-2475C>A
c.641C>A (p.Ser214Tyr)
c.596C>A (p.Ser199Tyr)
c.377-2475C>A (n.377-2475C>A)
2g.218890299C=CA1328965192WNT10Ac.692C= (p.Ser231=)
c.264-2475C=
c.641C= (p.Ser214=)
c.596C= (p.Ser199=)
c.377-2475C= (n.377-2475C=)
2g.218890299C>GCA2113999WNT10Ac.692C>G (p.Ser231Cys)
c.264-2475C>G
c.641C>G (p.Ser214Cys)
c.596C>G (p.Ser199Cys)
c.377-2475C>G (n.377-2475C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890299C>TCA350587284WNT10Ac.692C>T (p.Ser231Phe)
c.264-2475C>T
c.641C>T (p.Ser214Phe)
c.596C>T (p.Ser199Phe)
c.377-2475C>T (n.377-2475C>T)
 ClinVar dbSNP gnomAD v4
2g.218890301dupCA2740096466WNT10Ac.694dup (p.Arg232ProfsTer?)
c.264-2473dup
c.643dup (p.Arg215ProfsTer?)
c.598dup (p.Arg200ProfsTer?)
c.377-2473dup (n.377-2473dup)
 ClinVar
2g.218890301delCA915941719WNT10Ac.694del (p.Arg232GlyfsTer11)
c.264-2473del
c.643del (p.Arg215GlyfsTer11)
c.598del (p.Arg200GlyfsTer11)
c.377-2473del (n.377-2473del)
 ClinVar dbSNP gnomAD v4
2g.218890300C>ACA431416867WNT10Ac.693C>A (p.Ser231=)
c.264-2474C>A
c.642C>A (p.Ser214=)
c.597C>A (p.Ser199=)
c.377-2474C>A (n.377-2474C>A)
2g.218890300C=CA1328965194WNT10Ac.693C= (p.Ser231=)
c.264-2474C=
c.642C= (p.Ser214=)
c.597C= (p.Ser199=)
c.377-2474C= (n.377-2474C=)
2g.218890300C>GCA431416869WNT10Ac.693C>G (p.Ser231=)
c.264-2474C>G
c.642C>G (p.Ser214=)
c.597C>G (p.Ser199=)
c.377-2474C>G (n.377-2474C>G)
2g.218890300C>TCA2114000WNT10Ac.693C>T (p.Ser231=)
c.264-2474C>T
c.642C>T (p.Ser214=)
c.597C>T (p.Ser199=)
c.377-2474C>T (n.377-2474C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890301C>ACA431416871WNT10Ac.694C>A (p.Arg232=)
c.264-2473C>A
c.643C>A (p.Arg215=)
c.598C>A (p.Arg200=)
c.377-2473C>A (n.377-2473C>A)
2g.218890301C=CA1328965197WNT10Ac.694C= (p.Arg232=)
c.264-2473C=
c.643C= (p.Arg215=)
c.598C= (p.Arg200=)
c.377-2473C= (n.377-2473C=)
2g.218890301C>GCA350587292WNT10Ac.694C>G (p.Arg232Gly)
c.264-2473C>G
c.643C>G (p.Arg215Gly)
c.598C>G (p.Arg200Gly)
c.377-2473C>G (n.377-2473C>G)
 dbSNP gnomAD v2 gnomAD v4
2g.218890301C>TCA2114001WNT10Ac.694C>T (p.Arg232Trp)
c.264-2473C>T
c.643C>T (p.Arg215Trp)
c.598C>T (p.Arg200Trp)
c.377-2473C>T (n.377-2473C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890302G>ACA2114002WNT10Ac.695G>A (p.Arg232Gln)
c.264-2472G>A
c.644G>A (p.Arg215Gln)
c.599G>A (p.Arg200Gln)
c.377-2472G>A (n.377-2472G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890302G>CCA350587301WNT10Ac.695G>C (p.Arg232Pro)
c.264-2472G>C
c.644G>C (p.Arg215Pro)
c.599G>C (p.Arg200Pro)
c.377-2472G>C (n.377-2472G>C)
 gnomAD v4
2g.218890302G=CA1328965199WNT10Ac.695G= (p.Arg232=)
c.264-2472G=
c.644G= (p.Arg215=)
c.599G= (p.Arg200=)
c.377-2472G= (n.377-2472G=)
2g.218890302G>TCA350587302WNT10Ac.695G>T (p.Arg232Leu)
c.264-2472G>T
c.644G>T (p.Arg215Leu)
c.599G>T (p.Arg200Leu)
c.377-2472G>T (n.377-2472G>T)
 gnomAD v4
2g.218890303G>ACA2114003WNT10Ac.696G>A (p.Arg232=)
c.264-2471G>A
c.645G>A (p.Arg215=)
c.600G>A (p.Arg200=)
c.377-2471G>A (n.377-2471G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890303G>CCA431416872WNT10Ac.696G>C (p.Arg232=)
c.264-2471G>C
c.645G>C (p.Arg215=)
c.600G>C (p.Arg200=)
c.377-2471G>C (n.377-2471G>C)
2g.218890303G=CA1328965201WNT10Ac.696G= (p.Arg232=)
c.264-2471G=
c.645G= (p.Arg215=)
c.600G= (p.Arg200=)
c.377-2471G= (n.377-2471G=)
2g.218890303G>TCA431416874WNT10Ac.696G>T (p.Arg232=)
c.264-2471G>T
c.645G>T (p.Arg215=)
c.600G>T (p.Arg200=)
c.377-2471G>T (n.377-2471G>T)
2g.218890304G>ACA2114004WNT10Ac.697G>A (p.Glu233Lys)
c.264-2470G>A
c.646G>A (p.Glu216Lys)
c.601G>A (p.Glu201Lys)
c.377-2470G>A (n.377-2470G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890304G>CCA350587312WNT10Ac.697G>C (p.Glu233Gln)
c.264-2470G>C
c.646G>C (p.Glu216Gln)
c.601G>C (p.Glu201Gln)
c.377-2470G>C (n.377-2470G>C)
2g.218890304G=CA1328965204WNT10Ac.697G= (p.Glu233=)
c.264-2470G=
c.646G= (p.Glu216=)
c.601G= (p.Glu201=)
c.377-2470G= (n.377-2470G=)
2g.218890304G>TCA116863WNT10Ac.697G>T (p.Glu233Ter)
c.264-2470G>T
c.646G>T (p.Glu216Ter)
c.601G>T (p.Glu201Ter)
c.377-2470G>T (n.377-2470G>T)
 ClinVar dbSNP
2g.218890305A>CCA350587321WNT10Ac.698A>C (p.Glu233Ala)
c.264-2469A>C
c.647A>C (p.Glu216Ala)
c.602A>C (p.Glu201Ala)
c.377-2469A>C (n.377-2469A>C)
2g.218890305A>GCA350587324WNT10Ac.698A>G (p.Glu233Gly)
c.264-2469A>G
c.647A>G (p.Glu216Gly)
c.602A>G (p.Glu201Gly)
c.377-2469A>G (n.377-2469A>G)
 gnomAD v4
2g.218890305A>TCA350587319WNT10Ac.698A>T (p.Glu233Val)
c.264-2469A>T
c.647A>T (p.Glu216Val)
c.602A>T (p.Glu201Val)
c.377-2469A>T (n.377-2469A>T)
2g.218890306G>ACA431416880WNT10Ac.699G>A (p.Glu233=)
c.264-2468G>A
c.648G>A (p.Glu216=)
c.603G>A (p.Glu201=)
c.377-2468G>A (n.377-2468G>A)
 dbSNP
2g.218890306G>CCA350587330WNT10Ac.699G>C (p.Glu233Asp)
c.264-2468G>C
c.648G>C (p.Glu216Asp)
c.603G>C (p.Glu201Asp)
c.377-2468G>C (n.377-2468G>C)
2g.218890306G=CA1328965207WNT10Ac.699G= (p.Glu233=)
c.264-2468G=
c.648G= (p.Glu216=)
c.603G= (p.Glu201=)
c.377-2468G= (n.377-2468G=)
2g.218890306G>TCA350587328WNT10Ac.699G>T (p.Glu233Asp)
c.264-2468G>T
c.648G>T (p.Glu216Asp)
c.603G>T (p.Glu201Asp)
c.377-2468G>T (n.377-2468G>T)
2g.218890307C>ACA350587344WNT10Ac.700C>A (p.Pro234Thr)
c.264-2467C>A
c.649C>A (p.Pro217Thr)
c.604C>A (p.Pro202Thr)
c.377-2467C>A (n.377-2467C>A)
2g.218890307C>GCA350587351WNT10Ac.700C>G (p.Pro234Ala)
c.264-2467C>G
c.649C>G (p.Pro217Ala)
c.604C>G (p.Pro202Ala)
c.377-2467C>G (n.377-2467C>G)
2g.218890307C>TCA350587352WNT10Ac.700C>T (p.Pro234Ser)
c.264-2467C>T
c.649C>T (p.Pro217Ser)
c.604C>T (p.Pro202Ser)
c.377-2467C>T (n.377-2467C>T)
2g.218890308C>ACA2114005WNT10Ac.701C>A (p.Pro234His)
c.264-2466C>A
c.650C>A (p.Pro217His)
c.605C>A (p.Pro202His)
c.377-2466C>A (n.377-2466C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890308C=CA1328965209WNT10Ac.701C= (p.Pro234=)
c.264-2466C=
c.650C= (p.Pro217=)
c.605C= (p.Pro202=)
c.377-2466C= (n.377-2466C=)
2g.218890308C>GCA350587357WNT10Ac.701C>G (p.Pro234Arg)
c.264-2466C>G
c.650C>G (p.Pro217Arg)
c.605C>G (p.Pro202Arg)
c.377-2466C>G (n.377-2466C>G)
2g.218890308C>TCA350587361WNT10Ac.701C>T (p.Pro234Leu)
c.264-2466C>T
c.650C>T (p.Pro217Leu)
c.605C>T (p.Pro202Leu)
c.377-2466C>T (n.377-2466C>T)
2g.218890309T>ACA431416889WNT10Ac.702T>A (p.Pro234=)
c.264-2465T>A
c.651T>A (p.Pro217=)
c.606T>A (p.Pro202=)
c.377-2465T>A (n.377-2465T>A)
2g.218890309T>CCA431416891WNT10Ac.702T>C (p.Pro234=)
c.264-2465T>C
c.651T>C (p.Pro217=)
c.606T>C (p.Pro202=)
c.377-2465T>C (n.377-2465T>C)
2g.218890309T>GCA431416894WNT10Ac.702T>G (p.Pro234=)
c.264-2465T>G
c.651T>G (p.Pro217=)
c.606T>G (p.Pro202=)
c.377-2465T>G (n.377-2465T>G)
2g.218890310C>ACA350587364WNT10Ac.703C>A (p.His235Asn)
c.264-2464C>A
c.652C>A (p.His218Asn)
c.607C>A (p.His203Asn)
c.377-2464C>A (n.377-2464C>A)
2g.218890310C=CA1328965211WNT10Ac.703C= (p.His235=)
c.264-2464C=
c.652C= (p.His218=)
c.607C= (p.His203=)
c.377-2464C= (n.377-2464C=)
2g.218890310C>GCA350587366WNT10Ac.703C>G (p.His235Asp)
c.264-2464C>G
c.652C>G (p.His218Asp)
c.607C>G (p.His203Asp)
c.377-2464C>G (n.377-2464C>G)
2g.218890310C>TCA2114006WNT10Ac.703C>T (p.His235Tyr)
c.264-2464C>T
c.652C>T (p.His218Tyr)
c.607C>T (p.His203Tyr)
c.377-2464C>T (n.377-2464C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890311A>CCA350587370WNT10Ac.704A>C (p.His235Pro)
c.264-2463A>C
c.653A>C (p.His218Pro)
c.608A>C (p.His203Pro)
c.377-2463A>C (n.377-2463A>C)
2g.218890311A>GCA350587380WNT10Ac.704A>G (p.His235Arg)
c.264-2463A>G
c.653A>G (p.His218Arg)
c.608A>G (p.His203Arg)
c.377-2463A>G (n.377-2463A>G)
2g.218890311A>TCA350587387WNT10Ac.704A>T (p.His235Leu)
c.264-2463A>T
c.653A>T (p.His218Leu)
c.608A>T (p.His203Leu)
c.377-2463A>T (n.377-2463A>T)
2g.218890312C>ACA350587398WNT10Ac.705C>A (p.His235Gln)
c.264-2462C>A
c.654C>A (p.His218Gln)
c.609C>A (p.His203Gln)
c.377-2462C>A (n.377-2462C>A)
2g.218890312C=CA1328965213WNT10Ac.705C= (p.His235=)
c.264-2462C=
c.654C= (p.His218=)
c.609C= (p.His203=)
c.377-2462C= (n.377-2462C=)
2g.218890312C>GCA350587392WNT10Ac.705C>G (p.His235Gln)
c.264-2462C>G
c.654C>G (p.His218Gln)
c.609C>G (p.His203Gln)
c.377-2462C>G (n.377-2462C>G)
 gnomAD v4
2g.218890312C>TCA431416904WNT10Ac.705C>T (p.His235=)
c.264-2462C>T
c.654C>T (p.His218=)
c.609C>T (p.His203=)
c.377-2462C>T (n.377-2462C>T)
 ClinVar dbSNP
2g.218890313A>CCA431416906WNT10Ac.706A>C (p.Arg236=)
c.264-2461A>C
c.655A>C (p.Arg219=)
c.610A>C (p.Arg204=)
c.377-2461A>C (n.377-2461A>C)
2g.218890313A>GCA350587402WNT10Ac.706A>G (p.Arg236Gly)
c.264-2461A>G
c.655A>G (p.Arg219Gly)
c.610A>G (p.Arg204Gly)
c.377-2461A>G (n.377-2461A>G)
2g.218890313A>TCA350587405WNT10Ac.706A>T (p.Arg236Ter)
c.264-2461A>T
c.655A>T (p.Arg219Ter)
c.610A>T (p.Arg204Ter)
c.377-2461A>T (n.377-2461A>T)
2g.218890314G>ACA350587419WNT10Ac.707G>A (p.Arg236Lys)
c.264-2460G>A
c.656G>A (p.Arg219Lys)
c.611G>A (p.Arg204Lys)
c.377-2460G>A (n.377-2460G>A)
2g.218890314G>CCA350587421WNT10Ac.707G>C (p.Arg236Thr)
c.264-2460G>C
c.656G>C (p.Arg219Thr)
c.611G>C (p.Arg204Thr)
c.377-2460G>C (n.377-2460G>C)
2g.218890314G>TCA350587425WNT10Ac.707G>T (p.Arg236Ile)
c.264-2460G>T
c.656G>T (p.Arg219Ile)
c.611G>T (p.Arg204Ile)
c.377-2460G>T (n.377-2460G>T)
2g.218890315A>CCA350587429WNT10Ac.708A>C (p.Arg236Ser)
c.264-2459A>C
c.657A>C (p.Arg219Ser)
c.612A>C (p.Arg204Ser)
c.377-2459A>C (n.377-2459A>C)
2g.218890315A>GCA431416911WNT10Ac.708A>G (p.Arg236=)
c.264-2459A>G
c.657A>G (p.Arg219=)
c.612A>G (p.Arg204=)
c.377-2459A>G (n.377-2459A>G)
2g.218890315A>TCA350587431WNT10Ac.708A>T (p.Arg236Ser)
c.264-2459A>T
c.657A>T (p.Arg219Ser)
c.612A>T (p.Arg204Ser)
c.377-2459A>T (n.377-2459A>T)
2g.218890316G>ACA350587434WNT10Ac.709G>A (p.Asp237Asn)
c.264-2458G>A
c.658G>A (p.Asp220Asn)
c.613G>A (p.Asp205Asn)
c.377-2458G>A (n.377-2458G>A)
2g.218890316G>CCA350587436WNT10Ac.709G>C (p.Asp237His)
c.264-2458G>C
c.658G>C (p.Asp220His)
c.613G>C (p.Asp205His)
c.377-2458G>C (n.377-2458G>C)
2g.218890316G>TCA350587441WNT10Ac.709G>T (p.Asp237Tyr)
c.264-2458G>T
c.658G>T (p.Asp220Tyr)
c.613G>T (p.Asp205Tyr)
c.377-2458G>T (n.377-2458G>T)
2g.218890317A>CCA350587450WNT10Ac.710A>C (p.Asp237Ala)
c.264-2457A>C
c.659A>C (p.Asp220Ala)
c.614A>C (p.Asp205Ala)
c.377-2457A>C (n.377-2457A>C)
2g.218890317A>GCA350587451WNT10Ac.710A>G (p.Asp237Gly)
c.264-2457A>G
c.659A>G (p.Asp220Gly)
c.614A>G (p.Asp205Gly)
c.377-2457A>G (n.377-2457A>G)
2g.218890317A>TCA350587452WNT10Ac.710A>T (p.Asp237Val)
c.264-2457A>T
c.659A>T (p.Asp220Val)
c.614A>T (p.Asp205Val)
c.377-2457A>T (n.377-2457A>T)
2g.218890318C>ACA350587456WNT10Ac.711C>A (p.Asp237Glu)
c.264-2456C>A
c.660C>A (p.Asp220Glu)
c.615C>A (p.Asp205Glu)
c.377-2456C>A (n.377-2456C>A)
2g.218890318C=CA1328965216WNT10Ac.711C= (p.Asp237=)
c.264-2456C=
c.660C= (p.Asp220=)
c.615C= (p.Asp205=)
c.377-2456C= (n.377-2456C=)
2g.218890318C>GCA350587454WNT10Ac.711C>G (p.Asp237Glu)
c.264-2456C>G
c.660C>G (p.Asp220Glu)
c.615C>G (p.Asp205Glu)
c.377-2456C>G (n.377-2456C>G)
2g.218890318C>TCA431416915WNT10Ac.711C>T (p.Asp237=)
c.264-2456C>T
c.660C>T (p.Asp220=)
c.615C>T (p.Asp205=)
c.377-2456C>T (n.377-2456C>T)
 dbSNP
2g.218890319A=CA1328965218WNT10Ac.712A= (p.Ile238=)
c.264-2455A=
c.661A= (p.Ile221=)
c.616A= (p.Ile206=)
c.377-2455A= (n.377-2455A=)
2g.218890319A>CCA2114007WNT10Ac.712A>C (p.Ile238Leu)
c.264-2455A>C
c.661A>C (p.Ile221Leu)
c.616A>C (p.Ile206Leu)
c.377-2455A>C (n.377-2455A>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890319A>GCA2114008WNT10Ac.712A>G (p.Ile238Val)
c.264-2455A>G
c.661A>G (p.Ile221Val)
c.616A>G (p.Ile206Val)
c.377-2455A>G (n.377-2455A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890319A>TCA350587471WNT10Ac.712A>T (p.Ile238Phe)
c.264-2455A>T
c.661A>T (p.Ile221Phe)
c.616A>T (p.Ile206Phe)
c.377-2455A>T (n.377-2455A>T)
2g.218890320T>ACA350587475WNT10Ac.713T>A (p.Ile238Asn)
c.264-2454T>A
c.662T>A (p.Ile221Asn)
c.617T>A (p.Ile206Asn)
c.377-2454T>A (n.377-2454T>A)
2g.218890320T>CCA350587478WNT10Ac.713T>C (p.Ile238Thr)
c.264-2454T>C
c.662T>C (p.Ile221Thr)
c.617T>C (p.Ile206Thr)
c.377-2454T>C (n.377-2454T>C)
 gnomAD v4
2g.218890320T>GCA350587480WNT10Ac.713T>G (p.Ile238Ser)
c.264-2454T>G
c.662T>G (p.Ile221Ser)
c.617T>G (p.Ile206Ser)
c.377-2454T>G (n.377-2454T>G)
2g.218890321C>ACA431416920WNT10Ac.714C>A (p.Ile238=)
c.264-2453C>A
c.663C>A (p.Ile221=)
c.618C>A (p.Ile206=)
c.377-2453C>A (n.377-2453C>A)
 dbSNP gnomAD v3 gnomAD v4
2g.218890321C=CA1328965221WNT10Ac.714C= (p.Ile238=)
c.264-2453C=
c.663C= (p.Ile221=)
c.618C= (p.Ile206=)
c.377-2453C= (n.377-2453C=)
2g.218890321C>GCA350587483WNT10Ac.714C>G (p.Ile238Met)
c.264-2453C>G
c.663C>G (p.Ile221Met)
c.618C>G (p.Ile206Met)
c.377-2453C>G (n.377-2453C>G)
2g.218890321C>TCA431416921WNT10Ac.714C>T (p.Ile238=)
c.264-2453C>T
c.663C>T (p.Ile221=)
c.618C>T (p.Ile206=)
c.377-2453C>T (n.377-2453C>T)
2g.218890322C>ACA350587485WNT10Ac.715C>A (p.His239Asn)
c.264-2452C>A
c.664C>A (p.His222Asn)
c.619C>A (p.His207Asn)
c.377-2452C>A (n.377-2452C>A)
 dbSNP gnomAD v3 gnomAD v4
2g.218890322C=CA1328965223WNT10Ac.715C= (p.His239=)
c.264-2452C=
c.664C= (p.His222=)
c.619C= (p.His207=)
c.377-2452C= (n.377-2452C=)
2g.218890322C>GCA350587490WNT10Ac.715C>G (p.His239Asp)
c.264-2452C>G
c.664C>G (p.His222Asp)
c.619C>G (p.His207Asp)
c.377-2452C>G (n.377-2452C>G)
2g.218890322C>TCA350587492WNT10Ac.715C>T (p.His239Tyr)
c.264-2452C>T
c.664C>T (p.His222Tyr)
c.619C>T (p.His207Tyr)
c.377-2452C>T (n.377-2452C>T)
 ClinVar
2g.218890323A=CA1328965224WNT10Ac.716A= (p.His239=)
c.264-2451A=
c.665A= (p.His222=)
c.620A= (p.His207=)
c.377-2451A= (n.377-2451A=)
2g.218890323A>CCA350587497WNT10Ac.716A>C (p.His239Pro)
c.264-2451A>C
c.665A>C (p.His222Pro)
c.620A>C (p.His207Pro)
c.377-2451A>C (n.377-2451A>C)
2g.218890323A>GCA350587500WNT10Ac.716A>G (p.His239Arg)
c.264-2451A>G
c.665A>G (p.His222Arg)
c.620A>G (p.His207Arg)
c.377-2451A>G (n.377-2451A>G)
 dbSNP
2g.218890323A>TCA350587502WNT10Ac.716A>T (p.His239Leu)
c.264-2451A>T
c.665A>T (p.His222Leu)
c.620A>T (p.His207Leu)
c.377-2451A>T (n.377-2451A>T)
2g.218890323_218890324delinsACCA1328965226WNT10Ac.716_717delinsAC (p.His239=)
c.264-2451_264-2450delinsAC
c.665_666delinsAC (p.His222=)
c.620_621delinsAC (p.His207=)
c.377-2451_377-2450delinsAC (n.377-2451_377-2450delinsAC)
2g.218890324delCA916082289WNT10Ac.717del (p.His239GlnfsTer4)
c.264-2450del
c.666del (p.His222GlnfsTer4)
c.621del (p.His207GlnfsTer4)
c.377-2450del (n.377-2450del)
 ClinVar dbSNP
2g.218890324C>ACA350587510WNT10Ac.717C>A (p.His239Gln)
c.264-2450C>A
c.666C>A (p.His222Gln)
c.621C>A (p.His207Gln)
c.377-2450C>A (n.377-2450C>A)
 dbSNP
2g.218890324C=CA1328965227WNT10Ac.717C= (p.His239=)
c.264-2450C=
c.666C= (p.His222=)
c.621C= (p.His207=)
c.377-2450C= (n.377-2450C=)
2g.218890324C>GCA350587507WNT10Ac.717C>G (p.His239Gln)
c.264-2450C>G
c.666C>G (p.His222Gln)
c.621C>G (p.His207Gln)
c.377-2450C>G (n.377-2450C>G)
2g.218890324C>TCA2114009WNT10Ac.717C>T (p.His239=)
c.264-2450C>T
c.666C>T (p.His222=)
c.621C>T (p.His207=)
c.377-2450C>T (n.377-2450C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890325G>ACA350587512WNT10Ac.718G>A (p.Ala240Thr)
c.264-2449G>A
c.667G>A (p.Ala223Thr)
c.622G>A (p.Ala208Thr)
c.377-2449G>A (n.377-2449G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218890325G>CCA350587513WNT10Ac.718G>C (p.Ala240Pro)
c.264-2449G>C
c.667G>C (p.Ala223Pro)
c.622G>C (p.Ala208Pro)
c.377-2449G>C (n.377-2449G>C)
 gnomAD v4
2g.218890325G=CA1328965228WNT10Ac.718G= (p.Ala240=)
c.264-2449G=
c.667G= (p.Ala223=)
c.622G= (p.Ala208=)
c.377-2449G= (n.377-2449G=)
2g.218890325G>TCA350587514WNT10Ac.718G>T (p.Ala240Ser)
c.264-2449G>T
c.667G>T (p.Ala223Ser)
c.622G>T (p.Ala208Ser)
c.377-2449G>T (n.377-2449G>T)
 dbSNP gnomAD v4
2g.218890326C>ACA2114011WNT10Ac.719C>A (p.Ala240Glu)
c.264-2448C>A
c.668C>A (p.Ala223Glu)
c.623C>A (p.Ala208Glu)
c.377-2448C>A (n.377-2448C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890326C=CA1328965231WNT10Ac.719C= (p.Ala240=)
c.264-2448C=
c.668C= (p.Ala223=)
c.623C= (p.Ala208=)
c.377-2448C= (n.377-2448C=)
2g.218890326C>GCA350587525WNT10Ac.719C>G (p.Ala240Gly)
c.264-2448C>G
c.668C>G (p.Ala223Gly)
c.623C>G (p.Ala208Gly)
c.377-2448C>G (n.377-2448C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218890326C>TCA2114010WNT10Ac.719C>T (p.Ala240Val)
c.264-2448C>T
c.668C>T (p.Ala223Val)
c.623C>T (p.Ala208Val)
c.377-2448C>T (n.377-2448C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.218890327G>ACA2114012WNT10Ac.720G>A (p.Ala240=)
c.264-2447G>A
c.669G>A (p.Ala223=)
c.624G>A (p.Ala208=)
c.377-2447G>A (n.377-2447G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890327G>CCA431416936WNT10Ac.720G>C (p.Ala240=)
c.264-2447G>C
c.669G>C (p.Ala223=)
c.624G>C (p.Ala208=)
c.377-2447G>C (n.377-2447G>C)
2g.218890327G=CA1328965233WNT10Ac.720G= (p.Ala240=)
c.264-2447G=
c.669G= (p.Ala223=)
c.624G= (p.Ala208=)
c.377-2447G= (n.377-2447G=)
2g.218890327G>TCA431416934WNT10Ac.720G>T (p.Ala240=)
c.264-2447G>T
c.669G>T (p.Ala223=)
c.624G>T (p.Ala208=)
c.377-2447G>T (n.377-2447G>T)
 ClinVar dbSNP gnomAD v4
2g.218890328A>CCA431416938WNT10Ac.721A>C (p.Arg241=)
c.264-2446A>C
c.670A>C (p.Arg224=)
c.625A>C (p.Arg209=)
c.377-2446A>C (n.377-2446A>C)
2g.218890328A>GCA350587537WNT10Ac.721A>G (p.Arg241Gly)
c.264-2446A>G
c.670A>G (p.Arg224Gly)
c.625A>G (p.Arg209Gly)
c.377-2446A>G (n.377-2446A>G)
2g.218890328A>TCA350587541WNT10Ac.721A>T (p.Arg241Ter)
c.264-2446A>T
c.670A>T (p.Arg224Ter)
c.625A>T (p.Arg209Ter)
c.377-2446A>T (n.377-2446A>T)
2g.218890329G>ACA350587542WNT10Ac.722G>A (p.Arg241Lys)
c.264-2445G>A
c.671G>A (p.Arg224Lys)
c.626G>A (p.Arg209Lys)
c.377-2445G>A (n.377-2445G>A)
2g.218890329G>CCA350587543WNT10Ac.722G>C (p.Arg241Thr)
c.264-2445G>C
c.671G>C (p.Arg224Thr)
c.626G>C (p.Arg209Thr)
c.377-2445G>C (n.377-2445G>C)
2g.218890329G>TCA350587545WNT10Ac.722G>T (p.Arg241Ile)
c.264-2445G>T
c.671G>T (p.Arg224Ile)
c.626G>T (p.Arg209Ile)
c.377-2445G>T (n.377-2445G>T)
 gnomAD v4
2g.218890330A>CCA350587547WNT10Ac.723A>C (p.Arg241Ser)
c.264-2444A>C
c.672A>C (p.Arg224Ser)
c.627A>C (p.Arg209Ser)
c.377-2444A>C (n.377-2444A>C)
2g.218890330A>GCA431416948WNT10Ac.723A>G (p.Arg241=)
c.264-2444A>G
c.672A>G (p.Arg224=)
c.627A>G (p.Arg209=)
c.377-2444A>G (n.377-2444A>G)
2g.218890330A>TCA350587549WNT10Ac.723A>T (p.Arg241Ser)
c.264-2444A>T
c.672A>T (p.Arg224Ser)
c.627A>T (p.Arg209Ser)
c.377-2444A>T (n.377-2444A>T)
2g.218890331delCA2663174294WNT10Ac.724del (p.Met242Ter)
c.264-2443del
c.673del (p.Met225Ter)
c.628del (p.Met210Ter)
c.377-2443del (n.377-2443del)
 gnomAD v4
2g.218890331A=CA1328965235WNT10Ac.724A= (p.Met242=)
c.264-2443A=
c.673A= (p.Met225=)
c.628A= (p.Met210=)
c.377-2443A= (n.377-2443A=)
2g.218890331A>CCA350587569WNT10Ac.724A>C (p.Met242Leu)
c.264-2443A>C
c.673A>C (p.Met225Leu)
c.628A>C (p.Met210Leu)
c.377-2443A>C (n.377-2443A>C)
2g.218890331A>GCA2114013WNT10Ac.724A>G (p.Met242Val)
c.264-2443A>G
c.673A>G (p.Met225Val)
c.628A>G (p.Met210Val)
c.377-2443A>G (n.377-2443A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890331A>TCA350587568WNT10Ac.724A>T (p.Met242Leu)
c.264-2443A>T
c.673A>T (p.Met225Leu)
c.628A>T (p.Met210Leu)
c.377-2443A>T (n.377-2443A>T)
2g.218890332T>ACA2114015WNT10Ac.725T>A (p.Met242Lys)
c.264-2442T>A
c.674T>A (p.Met225Lys)
c.629T>A (p.Met210Lys)
c.377-2442T>A (n.377-2442T>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890332T>CCA2114014WNT10Ac.725T>C (p.Met242Thr)
c.264-2442T>C
c.674T>C (p.Met225Thr)
c.629T>C (p.Met210Thr)
c.377-2442T>C (n.377-2442T>C)
 dbSNP ExAC gnomAD v3 gnomAD v4
2g.218890332T>GCA350587585WNT10Ac.725T>G (p.Met242Arg)
c.264-2442T>G
c.674T>G (p.Met225Arg)
c.629T>G (p.Met210Arg)
c.377-2442T>G (n.377-2442T>G)
 ClinVar dbSNP
2g.218890332T=CA1328965238WNT10Ac.725T= (p.Met242=)
c.264-2442T=
c.674T= (p.Met225=)
c.629T= (p.Met210=)
c.377-2442T= (n.377-2442T=)
2g.218890333G>ACA2114016WNT10Ac.726G>A (p.Met242Ile)
c.264-2441G>A
c.675G>A (p.Met225Ile)
c.630G>A (p.Met210Ile)
c.377-2441G>A (n.377-2441G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890333G>CCA350587596WNT10Ac.726G>C (p.Met242Ile)
c.264-2441G>C
c.675G>C (p.Met225Ile)
c.630G>C (p.Met210Ile)
c.377-2441G>C (n.377-2441G>C)
2g.218890333G=CA1328965241WNT10Ac.726G= (p.Met242=)
c.264-2441G=
c.675G= (p.Met225=)
c.630G= (p.Met210=)
c.377-2441G= (n.377-2441G=)
2g.218890333G>TCA350587598WNT10Ac.726G>T (p.Met242Ile)
c.264-2441G>T
c.675G>T (p.Met225Ile)
c.630G>T (p.Met210Ile)
c.377-2441G>T (n.377-2441G>T)
2g.218890334A>CCA431416955WNT10Ac.727A>C (p.Arg243=)
c.264-2440A>C
c.676A>C (p.Arg226=)
c.631A>C (p.Arg211=)
c.377-2440A>C (n.377-2440A>C)
2g.218890334A>GCA350587601WNT10Ac.727A>G (p.Arg243Gly)
c.264-2440A>G
c.676A>G (p.Arg226Gly)
c.631A>G (p.Arg211Gly)
c.377-2440A>G (n.377-2440A>G)
 gnomAD v4
2g.218890334A>TCA350587613WNT10Ac.727A>T (p.Arg243Trp)
c.264-2440A>T
c.676A>T (p.Arg226Trp)
c.631A>T (p.Arg211Trp)
c.377-2440A>T (n.377-2440A>T)
2g.218890335G>ACA350587617WNT10Ac.728G>A (p.Arg243Lys)
c.264-2439G>A
c.677G>A (p.Arg226Lys)
c.632G>A (p.Arg211Lys)
c.377-2439G>A (n.377-2439G>A)
 dbSNP
2g.218890335G>CCA350587620WNT10Ac.728G>C (p.Arg243Thr)
c.264-2439G>C
c.677G>C (p.Arg226Thr)
c.632G>C (p.Arg211Thr)
c.377-2439G>C (n.377-2439G>C)
2g.218890335G=CA1328965243WNT10Ac.728G= (p.Arg243=)
c.264-2439G=
c.677G= (p.Arg226=)
c.632G= (p.Arg211=)
c.377-2439G= (n.377-2439G=)
2g.218890335G>TCA350587623WNT10Ac.728G>T (p.Arg243Met)
c.264-2439G>T
c.677G>T (p.Arg226Met)
c.632G>T (p.Arg211Met)
c.377-2439G>T (n.377-2439G>T)
2g.218890336G>ACA431416963WNT10Ac.729G>A (p.Arg243=)
c.264-2438G>A
c.678G>A (p.Arg226=)
c.633G>A (p.Arg211=)
c.377-2438G>A (n.377-2438G>A)
2g.218890336G>CCA350587635WNT10Ac.729G>C (p.Arg243Ser)
c.264-2438G>C
c.678G>C (p.Arg226Ser)
c.633G>C (p.Arg211Ser)
c.377-2438G>C (n.377-2438G>C)
 dbSNP
2g.218890336G=CA1328965245WNT10Ac.729G= (p.Arg243=)
c.264-2438G=
c.678G= (p.Arg226=)
c.633G= (p.Arg211=)
c.377-2438G= (n.377-2438G=)
2g.218890336G>TCA350587639WNT10Ac.729G>T (p.Arg243Ser)
c.264-2438G>T
c.678G>T (p.Arg226Ser)
c.633G>T (p.Arg211Ser)
c.377-2438G>T (n.377-2438G>T)
 dbSNP gnomAD v3 gnomAD v4
2g.218890337C>ACA350587642WNT10Ac.730C>A (p.Leu244Ile)
c.264-2437C>A
c.679C>A (p.Leu227Ile)
c.634C>A (p.Leu212Ile)
c.377-2437C>A (n.377-2437C>A)
2g.218890337C=CA1328965247WNT10Ac.730C= (p.Leu244=)
c.264-2437C=
c.679C= (p.Leu227=)
c.634C= (p.Leu212=)
c.377-2437C= (n.377-2437C=)
2g.218890337C>GCA350587640WNT10Ac.730C>G (p.Leu244Val)
c.264-2437C>G
c.679C>G (p.Leu227Val)
c.634C>G (p.Leu212Val)
c.377-2437C>G (n.377-2437C>G)
2g.218890337C>TCA2114017WNT10Ac.730C>T (p.Leu244Phe)
c.264-2437C>T
c.679C>T (p.Leu227Phe)
c.634C>T (p.Leu212Phe)
c.377-2437C>T (n.377-2437C>T)
 dbSNP ExAC gnomAD v4
2g.218890338T>ACA350587645WNT10Ac.731T>A (p.Leu244His)
c.264-2436T>A
c.680T>A (p.Leu227His)
c.635T>A (p.Leu212His)
c.377-2436T>A (n.377-2436T>A)
2g.218890338T>CCA350587647WNT10Ac.731T>C (p.Leu244Pro)
c.264-2436T>C
c.680T>C (p.Leu227Pro)
c.635T>C (p.Leu212Pro)
c.377-2436T>C (n.377-2436T>C)
2g.218890338T>GCA350587650WNT10Ac.731T>G (p.Leu244Arg)
c.264-2436T>G
c.680T>G (p.Leu227Arg)
c.635T>G (p.Leu212Arg)
c.377-2436T>G (n.377-2436T>G)
2g.218890339T>ACA431416974WNT10Ac.732T>A (p.Leu244=)
c.264-2435T>A
c.681T>A (p.Leu227=)
c.636T>A (p.Leu212=)
c.377-2435T>A (n.377-2435T>A)
2g.218890339T>CCA431416975WNT10Ac.732T>C (p.Leu244=)
c.264-2435T>C
c.681T>C (p.Leu227=)
c.636T>C (p.Leu212=)
c.377-2435T>C (n.377-2435T>C)
2g.218890339T>GCA2114018WNT10Ac.732T>G (p.Leu244=)
c.264-2435T>G
c.681T>G (p.Leu227=)
c.636T>G (p.Leu212=)
c.377-2435T>G (n.377-2435T>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890339T=CA1328965249WNT10Ac.732T= (p.Leu244=)
c.264-2435T=
c.681T= (p.Leu227=)
c.636T= (p.Leu212=)
c.377-2435T= (n.377-2435T=)
2g.218890340C>ACA350587656WNT10Ac.733C>A (p.His245Asn)
c.264-2434C>A
c.682C>A (p.His228Asn)
c.637C>A (p.His213Asn)
c.377-2434C>A (n.377-2434C>A)
2g.218890340C=CA1328965250WNT10Ac.733C= (p.His245=)
c.264-2434C=
c.682C= (p.His228=)
c.637C= (p.His213=)
c.377-2434C= (n.377-2434C=)
2g.218890340C>GCA350587667WNT10Ac.733C>G (p.His245Asp)
c.264-2434C>G
c.682C>G (p.His228Asp)
c.637C>G (p.His213Asp)
c.377-2434C>G (n.377-2434C>G)
2g.218890340C>TCA350587674WNT10Ac.733C>T (p.His245Tyr)
c.264-2434C>T
c.682C>T (p.His228Tyr)
c.637C>T (p.His213Tyr)
c.377-2434C>T (n.377-2434C>T)
 dbSNP gnomAD v4
2g.218890341A=CA1328965252WNT10Ac.734A= (p.His245=)
c.264-2433A=
c.683A= (p.His228=)
c.638A= (p.His213=)
c.377-2433A= (n.377-2433A=)
2g.218890341A>CCA350587677WNT10Ac.734A>C (p.His245Pro)
c.264-2433A>C
c.683A>C (p.His228Pro)
c.638A>C (p.His213Pro)
c.377-2433A>C (n.377-2433A>C)
2g.218890341A>GCA2114019WNT10Ac.734A>G (p.His245Arg)
c.264-2433A>G
c.683A>G (p.His228Arg)
c.638A>G (p.His213Arg)
c.377-2433A>G (n.377-2433A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890341A>TCA350587683WNT10Ac.734A>T (p.His245Leu)
c.264-2433A>T
c.683A>T (p.His228Leu)
c.638A>T (p.His213Leu)
c.377-2433A>T (n.377-2433A>T)
2g.218890342C>ACA350587687WNT10Ac.735C>A (p.His245Gln)
c.264-2432C>A
c.684C>A (p.His228Gln)
c.639C>A (p.His213Gln)
c.377-2432C>A (n.377-2432C>A)
2g.218890342C>GCA350587689WNT10Ac.735C>G (p.His245Gln)
c.264-2432C>G
c.684C>G (p.His228Gln)
c.639C>G (p.His213Gln)
c.377-2432C>G (n.377-2432C>G)
2g.218890342C>TCA431416979WNT10Ac.735C>T (p.His245=)
c.264-2432C>T
c.684C>T (p.His228=)
c.639C>T (p.His213=)
c.377-2432C>T (n.377-2432C>T)
 COSMIC
2g.218890343A=CA1328965253WNT10Ac.736A= (p.Asn246=)
c.264-2431A=
c.685A= (p.Asn229=)
c.640A= (p.Asn214=)
c.377-2431A= (n.377-2431A=)
2g.218890343A>CCA350587697WNT10Ac.736A>C (p.Asn246His)
c.264-2431A>C
c.685A>C (p.Asn229His)
c.640A>C (p.Asn214His)
c.377-2431A>C (n.377-2431A>C)
2g.218890343A>GCA350587700WNT10Ac.736A>G (p.Asn246Asp)
c.264-2431A>G
c.685A>G (p.Asn229Asp)
c.640A>G (p.Asn214Asp)
c.377-2431A>G (n.377-2431A>G)
 dbSNP gnomAD v2 gnomAD v4
2g.218890343A>TCA350587692WNT10Ac.736A>T (p.Asn246Tyr)
c.264-2431A>T
c.685A>T (p.Asn229Tyr)
c.640A>T (p.Asn214Tyr)
c.377-2431A>T (n.377-2431A>T)
2g.218890344A=CA1328965255WNT10Ac.737A= (p.Asn246=)
c.264-2430A=
c.686A= (p.Asn229=)
c.641A= (p.Asn214=)
c.377-2430A= (n.377-2430A=)
2g.218890344A>CCA350587730WNT10Ac.737A>C (p.Asn246Thr)
c.264-2430A>C
c.686A>C (p.Asn229Thr)
c.641A>C (p.Asn214Thr)
c.377-2430A>C (n.377-2430A>C)
2g.218890344A>GCA65917054WNT10Ac.737A>G (p.Asn246Ser)
c.264-2430A>G
c.686A>G (p.Asn229Ser)
c.641A>G (p.Asn214Ser)
c.377-2430A>G (n.377-2430A>G)
 dbSNP gnomAD v3 gnomAD v4
2g.218890344A>TCA350587741WNT10Ac.737A>T (p.Asn246Ile)
c.264-2430A>T
c.686A>T (p.Asn229Ile)
c.641A>T (p.Asn214Ile)
c.377-2430A>T (n.377-2430A>T)
2g.218890345C>ACA350587745WNT10Ac.738C>A (p.Asn246Lys)
c.264-2429C>A
c.687C>A (p.Asn229Lys)
c.642C>A (p.Asn214Lys)
c.377-2429C>A (n.377-2429C>A)
2g.218890345C=CA1328965257WNT10Ac.738C= (p.Asn246=)
c.264-2429C=
c.687C= (p.Asn229=)
c.642C= (p.Asn214=)
c.377-2429C= (n.377-2429C=)
2g.218890345C>GCA350587746WNT10Ac.738C>G (p.Asn246Lys)
c.264-2429C>G
c.687C>G (p.Asn229Lys)
c.642C>G (p.Asn214Lys)
c.377-2429C>G (n.377-2429C>G)
2g.218890345C>TCA2114020WNT10Ac.738C>T (p.Asn246=)
c.264-2429C>T
c.687C>T (p.Asn229=)
c.642C>T (p.Asn214=)
c.377-2429C>T (n.377-2429C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890346A>CCA350587747WNT10Ac.739A>C (p.Asn247His)
c.264-2428A>C
c.688A>C (p.Asn230His)
c.643A>C (p.Asn215His)
c.377-2428A>C (n.377-2428A>C)
2g.218890346A>GCA350587750WNT10Ac.739A>G (p.Asn247Asp)
c.264-2428A>G
c.688A>G (p.Asn230Asp)
c.643A>G (p.Asn215Asp)
c.377-2428A>G (n.377-2428A>G)
2g.218890346A>TCA350587752WNT10Ac.739A>T (p.Asn247Tyr)
c.264-2428A>T
c.688A>T (p.Asn230Tyr)
c.643A>T (p.Asn215Tyr)
c.377-2428A>T (n.377-2428A>T)
2g.218890347A>CCA350587755WNT10Ac.740A>C (p.Asn247Thr)
c.264-2427A>C
c.689A>C (p.Asn230Thr)
c.644A>C (p.Asn215Thr)
c.377-2427A>C (n.377-2427A>C)
2g.218890347A>GCA350587773WNT10Ac.740A>G (p.Asn247Ser)
c.264-2427A>G
c.689A>G (p.Asn230Ser)
c.644A>G (p.Asn215Ser)
c.377-2427A>G (n.377-2427A>G)
2g.218890347A>TCA350587778WNT10Ac.740A>T (p.Asn247Ile)
c.264-2427A>T
c.689A>T (p.Asn230Ile)
c.644A>T (p.Asn215Ile)
c.377-2427A>T (n.377-2427A>T)
2g.218890347_218890349delCA2754310515WNT10Ac.740_742del (p.Asn247del)
c.264-2427_264-2425del
c.689_691del (p.Asn230del)
c.644_646del (p.Asn215del)
c.377-2427_377-2425del (n.377-2427_377-2425del)
2g.218890348C>ACA350587782WNT10Ac.741C>A (p.Asn247Lys)
c.264-2426C>A
c.690C>A (p.Asn230Lys)
c.645C>A (p.Asn215Lys)
c.377-2426C>A (n.377-2426C>A)
2g.218890348C=CA1328965259WNT10Ac.741C= (p.Asn247=)
c.264-2426C=
c.690C= (p.Asn230=)
c.645C= (p.Asn215=)
c.377-2426C= (n.377-2426C=)
2g.218890348C>GCA350587785WNT10Ac.741C>G (p.Asn247Lys)
c.264-2426C>G
c.690C>G (p.Asn230Lys)
c.645C>G (p.Asn215Lys)
c.377-2426C>G (n.377-2426C>G)
 dbSNP gnomAD v4
2g.218890348C>TCA431416987WNT10Ac.741C>T (p.Asn247=)
c.264-2426C>T
c.690C>T (p.Asn230=)
c.645C>T (p.Asn215=)
c.377-2426C>T (n.377-2426C>T)
 ClinVar gnomAD v4
2g.218890349C>ACA431416988WNT10Ac.742C>A (p.Arg248=)
c.264-2425C>A
c.691C>A (p.Arg231=)
c.646C>A (p.Arg216=)
c.377-2425C>A (n.377-2425C>A)
2g.218890349C=CA1328965262WNT10Ac.742C= (p.Arg248=)
c.264-2425C=
c.691C= (p.Arg231=)
c.646C= (p.Arg216=)
c.377-2425C= (n.377-2425C=)
2g.218890349C>GCA350587786WNT10Ac.742C>G (p.Arg248Gly)
c.264-2425C>G
c.691C>G (p.Arg231Gly)
c.646C>G (p.Arg216Gly)
c.377-2425C>G (n.377-2425C>G)
2g.218890349C>TCA10588338WNT10Ac.742C>T (p.Arg248Ter)
c.264-2425C>T
c.691C>T (p.Arg231Ter)
c.646C>T (p.Arg216Ter)
c.377-2425C>T (n.377-2425C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218890350G>ACA2114021WNT10Ac.743G>A (p.Arg248Gln)
c.264-2424G>A
c.692G>A (p.Arg231Gln)
c.647G>A (p.Arg216Gln)
c.377-2424G>A (n.377-2424G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890350G>CCA350587792WNT10Ac.743G>C (p.Arg248Pro)
c.264-2424G>C
c.692G>C (p.Arg231Pro)
c.647G>C (p.Arg216Pro)
c.377-2424G>C (n.377-2424G>C)
2g.218890350G=CA1328965263WNT10Ac.743G= (p.Arg248=)
c.264-2424G=
c.692G= (p.Arg231=)
c.647G= (p.Arg216=)
c.377-2424G= (n.377-2424G=)
2g.218890350G>TCA350587793WNT10Ac.743G>T (p.Arg248Leu)
c.264-2424G>T
c.692G>T (p.Arg231Leu)
c.647G>T (p.Arg216Leu)
c.377-2424G>T (n.377-2424G>T)
 dbSNP gnomAD v4
2g.218890351A=CA1328965265WNT10Ac.744A= (p.Arg248=)
c.264-2423A=
c.693A= (p.Arg231=)
c.648A= (p.Arg216=)
c.377-2423A= (n.377-2423A=)
2g.218890351A>CCA431416992WNT10Ac.744A>C (p.Arg248=)
c.264-2423A>C
c.693A>C (p.Arg231=)
c.648A>C (p.Arg216=)
c.377-2423A>C (n.377-2423A>C)
2g.218890351A>GCA431416993WNT10Ac.744A>G (p.Arg248=)
c.264-2423A>G
c.693A>G (p.Arg231=)
c.648A>G (p.Arg216=)
c.377-2423A>G (n.377-2423A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218890351A>TCA431416994WNT10Ac.744A>T (p.Arg248=)
c.264-2423A>T
c.693A>T (p.Arg231=)
c.648A>T (p.Arg216=)
c.377-2423A>T (n.377-2423A>T)
2g.218890352G>ACA2114022WNT10Ac.745G>A (p.Val249Ile)
c.264-2422G>A
c.694G>A (p.Val232Ile)
c.649G>A (p.Val217Ile)
c.377-2422G>A (n.377-2422G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890352G>CCA350587795WNT10Ac.745G>C (p.Val249Leu)
c.264-2422G>C
c.694G>C (p.Val232Leu)
c.649G>C (p.Val217Leu)
c.377-2422G>C (n.377-2422G>C)
2g.218890352G=CA1328965267WNT10Ac.745G= (p.Val249=)
c.264-2422G=
c.694G= (p.Val232=)
c.649G= (p.Val217=)
c.377-2422G= (n.377-2422G=)
2g.218890352G>TCA350587797WNT10Ac.745G>T (p.Val249Phe)
c.264-2422G>T
c.694G>T (p.Val232Phe)
c.649G>T (p.Val217Phe)
c.377-2422G>T (n.377-2422G>T)
2g.218890353T>ACA350587803WNT10Ac.746T>A (p.Val249Asp)
c.264-2421T>A
c.695T>A (p.Val232Asp)
c.650T>A (p.Val217Asp)
c.377-2421T>A (n.377-2421T>A)
2g.218890353T>CCA2114023WNT10Ac.746T>C (p.Val249Ala)
c.264-2421T>C
c.695T>C (p.Val232Ala)
c.650T>C (p.Val217Ala)
c.377-2421T>C (n.377-2421T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890353T>GCA350587807WNT10Ac.746T>G (p.Val249Gly)
c.264-2421T>G
c.695T>G (p.Val232Gly)
c.650T>G (p.Val217Gly)
c.377-2421T>G (n.377-2421T>G)
2g.218890353T=CA1328965269WNT10Ac.746T= (p.Val249=)
c.264-2421T=
c.695T= (p.Val232=)
c.650T= (p.Val217=)
c.377-2421T= (n.377-2421T=)
2g.218890354T>ACA431417002WNT10Ac.747T>A (p.Val249=)
c.264-2420T>A
c.696T>A (p.Val232=)
c.651T>A (p.Val217=)
c.377-2420T>A (n.377-2420T>A)
 dbSNP gnomAD v2 gnomAD v4
2g.218890354T>CCA431417001WNT10Ac.747T>C (p.Val249=)
c.264-2420T>C
c.696T>C (p.Val232=)
c.651T>C (p.Val217=)
c.377-2420T>C (n.377-2420T>C)
2g.218890354T>GCA431417000WNT10Ac.747T>G (p.Val249=)
c.264-2420T>G
c.696T>G (p.Val232=)
c.651T>G (p.Val217=)
c.377-2420T>G (n.377-2420T>G)
2g.218890354T=CA1328965271WNT10Ac.747T= (p.Val249=)
c.264-2420T=
c.696T= (p.Val232=)
c.651T= (p.Val217=)
c.377-2420T= (n.377-2420T=)
2g.218890355G>ACA350587811WNT10Ac.748G>A (p.Gly250Arg)
c.264-2419G>A
c.697G>A (p.Gly233Arg)
c.652G>A (p.Gly218Arg)
c.377-2419G>A (n.377-2419G>A)
 dbSNP
2g.218890355G>CCA65917073WNT10Ac.748G>C (p.Gly250Arg)
c.264-2419G>C
c.697G>C (p.Gly233Arg)
c.652G>C (p.Gly218Arg)
c.377-2419G>C (n.377-2419G>C)
 dbSNP gnomAD v3 gnomAD v4
2g.218890355G=CA1328965273WNT10Ac.748G= (p.Gly250=)
c.264-2419G=
c.697G= (p.Gly233=)
c.652G= (p.Gly218=)
c.377-2419G= (n.377-2419G=)
2g.218890355G>TCA350587823WNT10Ac.748G>T (p.Gly250Trp)
c.264-2419G>T
c.697G>T (p.Gly233Trp)
c.652G>T (p.Gly218Trp)
c.377-2419G>T (n.377-2419G>T)
2g.218890356G>ACA350587837WNT10Ac.749G>A (p.Gly250Glu)
c.264-2418G>A
c.698G>A (p.Gly233Glu)
c.653G>A (p.Gly218Glu)
c.377-2418G>A (n.377-2418G>A)
2g.218890356G>CCA350587834WNT10Ac.749G>C (p.Gly250Ala)
c.264-2418G>C
c.698G>C (p.Gly233Ala)
c.653G>C (p.Gly218Ala)
c.377-2418G>C (n.377-2418G>C)
2g.218890356G>TCA350587830WNT10Ac.749G>T (p.Gly250Val)
c.264-2418G>T
c.698G>T (p.Gly233Val)
c.653G>T (p.Gly218Val)
c.377-2418G>T (n.377-2418G>T)
2g.218890357G>ACA431417008WNT10Ac.750G>A (p.Gly250=)
c.264-2417G>A
c.699G>A (p.Gly233=)
c.654G>A (p.Gly218=)
c.377-2417G>A (n.377-2417G>A)
2g.218890357G>CCA431417009WNT10Ac.750G>C (p.Gly250=)
c.264-2417G>C
c.699G>C (p.Gly233=)
c.654G>C (p.Gly218=)
c.377-2417G>C (n.377-2417G>C)
2g.218890357G>TCA431417010WNT10Ac.750G>T (p.Gly250=)
c.264-2417G>T
c.699G>T (p.Gly233=)
c.654G>T (p.Gly218=)
c.377-2417G>T (n.377-2417G>T)
2g.218890358A=CA1328965275WNT10Ac.751A= (p.Arg251=)
c.264-2416A=
c.700A= (p.Arg234=)
c.655A= (p.Arg219=)
c.377-2416A= (n.377-2416A=)
2g.218890358A>CCA431417011WNT10Ac.751A>C (p.Arg251=)
c.264-2416A>C
c.700A>C (p.Arg234=)
c.655A>C (p.Arg219=)
c.377-2416A>C (n.377-2416A>C)
2g.218890358A>GCA2114024WNT10Ac.751A>G (p.Arg251Gly)
c.264-2416A>G
c.700A>G (p.Arg234Gly)
c.655A>G (p.Arg219Gly)
c.377-2416A>G (n.377-2416A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218890358A>TCA350587843WNT10Ac.751A>T (p.Arg251Trp)
c.264-2416A>T
c.700A>T (p.Arg234Trp)
c.655A>T (p.Arg219Trp)
c.377-2416A>T (n.377-2416A>T)
2g.218890359G>ACA350587845WNT10Ac.752G>A (p.Arg251Lys)
c.264-2415G>A
c.701G>A (p.Arg234Lys)
c.656G>A (p.Arg219Lys)
c.377-2415G>A (n.377-2415G>A)
2g.218890359G>CCA350587852WNT10Ac.752G>C (p.Arg251Thr)
c.264-2415G>C
c.701G>C (p.Arg234Thr)
c.656G>C (p.Arg219Thr)
c.377-2415G>C (n.377-2415G>C)
2g.218890359G=CA1328965277WNT10Ac.752G= (p.Arg251=)
c.264-2415G=
c.701G= (p.Arg234=)
c.656G= (p.Arg219=)
c.377-2415G= (n.377-2415G=)
2g.218890359G>TCA350587847WNT10Ac.752G>T (p.Arg251Met)
c.264-2415G>T
c.701G>T (p.Arg234Met)
c.656G>T (p.Arg219Met)
c.377-2415G>T (n.377-2415G>T)
 dbSNP gnomAD v4
2g.218890360G>ACA431417016WNT10Ac.753G>A (p.Arg251=)
c.264-2414G>A
c.702G>A (p.Arg234=)
c.657G>A (p.Arg219=)
c.377-2414G>A (n.377-2414G>A)
2g.218890360G>CCA350587856WNT10Ac.753G>C (p.Arg251Ser)
c.264-2414G>C
c.702G>C (p.Arg234Ser)
c.657G>C (p.Arg219Ser)
c.377-2414G>C (n.377-2414G>C)
2g.218890360G>TCA350587868WNT10Ac.753G>T (p.Arg251Ser)
c.264-2414G>T
c.702G>T (p.Arg234Ser)
c.657G>T (p.Arg219Ser)
c.377-2414G>T (n.377-2414G>T)
2g.218890361C>ACA350587873WNT10Ac.754C>A (p.Gln252Lys)
c.264-2413C>A
c.703C>A (p.Gln235Lys)
c.658C>A (p.Gln220Lys)
c.377-2413C>A (n.377-2413C>A)
2g.218890361C>GCA350587878WNT10Ac.754C>G (p.Gln252Glu)
c.264-2413C>G
c.703C>G (p.Gln235Glu)
c.658C>G (p.Gln220Glu)
c.377-2413C>G (n.377-2413C>G)
2g.218890361C>TCA350587875WNT10Ac.754C>T (p.Gln252Ter)
c.264-2413C>T
c.703C>T (p.Gln235Ter)
c.658C>T (p.Gln220Ter)
c.377-2413C>T (n.377-2413C>T)
2g.218890362A>CCA350587879WNT10Ac.755A>C (p.Gln252Pro)
c.264-2412A>C
c.704A>C (p.Gln235Pro)
c.659A>C (p.Gln220Pro)
c.377-2412A>C (n.377-2412A>C)
2g.218890362A>GCA350587880WNT10Ac.755A>G (p.Gln252Arg)
c.264-2412A>G
c.704A>G (p.Gln235Arg)
c.659A>G (p.Gln220Arg)
c.377-2412A>G (n.377-2412A>G)
2g.218890362A>TCA350587881WNT10Ac.755A>T (p.Gln252Leu)
c.264-2412A>T
c.704A>T (p.Gln235Leu)
c.659A>T (p.Gln220Leu)
c.377-2412A>T (n.377-2412A>T)

Number of alleles fetched