Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.218890249_218890261delCA2663174291WNT10Ac.642_654del (p.Cys214TrpfsTer25)
c.264-2525_264-2513del
c.591_603del (p.Cys197TrpfsTer25)
c.546_558del (p.Cys182TrpfsTer25)
c.377-2525_377-2513del (n.377-2525_377-2513del)
gnomAD v4
2g.218890257A=CA1328965128WNT10Ac.650A= (p.Asp217=)
c.264-2517A=
c.599A= (p.Asp200=)
c.554A= (p.Asp185=)
c.377-2517A= (n.377-2517A=)
2g.218890257A>CCA350586944WNT10Ac.650A>C (p.Asp217Ala)
c.264-2517A>C
c.599A>C (p.Asp200Ala)
c.554A>C (p.Asp185Ala)
c.377-2517A>C (n.377-2517A>C)
2g.218890257A>GCA16604387WNT10Ac.650A>G (p.Asp217Gly)
c.264-2517A>G
c.599A>G (p.Asp200Gly)
c.554A>G (p.Asp185Gly)
c.377-2517A>G (n.377-2517A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218890257A>TCA350586961WNT10Ac.650A>T (p.Asp217Val)
c.264-2517A>T
c.599A>T (p.Asp200Val)
c.554A>T (p.Asp185Val)
c.377-2517A>T (n.377-2517A>T)
2g.218890258C>ACA350586966WNT10Ac.651C>A (p.Asp217Glu)
c.264-2516C>A
c.600C>A (p.Asp200Glu)
c.555C>A (p.Asp185Glu)
c.377-2516C>A (n.377-2516C>A)
2g.218890258C>GCA350586967WNT10Ac.651C>G (p.Asp217Glu)
c.264-2516C>G
c.600C>G (p.Asp200Glu)
c.555C>G (p.Asp185Glu)
c.377-2516C>G (n.377-2516C>G)
2g.218890258C>TCA431416789WNT10Ac.651C>T (p.Asp217=)
c.264-2516C>T
c.600C>T (p.Asp200=)
c.555C>T (p.Asp185=)
c.377-2516C>T (n.377-2516C>T)
gnomAD v4
2g.218890259A=CA1328965129WNT10Ac.652A= (p.Met218=)
c.264-2515A=
c.601A= (p.Met201=)
c.556A= (p.Met186=)
c.377-2515A= (n.377-2515A=)
2g.218890259A>CCA65916870WNT10Ac.652A>C (p.Met218Leu)
c.264-2515A>C
c.601A>C (p.Met201Leu)
c.556A>C (p.Met186Leu)
c.377-2515A>C (n.377-2515A>C)
dbSNP gnomAD v2 gnomAD v4
2g.218890259A>GCA2113987WNT10Ac.652A>G (p.Met218Val)
c.264-2515A>G
c.601A>G (p.Met201Val)
c.556A>G (p.Met186Val)
c.377-2515A>G (n.377-2515A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890259A>TCA350586978WNT10Ac.652A>T (p.Met218Leu)
c.264-2515A>T
c.601A>T (p.Met201Leu)
c.556A>T (p.Met186Leu)
c.377-2515A>T (n.377-2515A>T)
2g.218890260T>ACA350586981WNT10Ac.653T>A (p.Met218Lys)
c.264-2514T>A
c.602T>A (p.Met201Lys)
c.557T>A (p.Met186Lys)
c.377-2514T>A (n.377-2514T>A)
2g.218890260T>CCA2113988WNT10Ac.653T>C (p.Met218Thr)
c.264-2514T>C
c.602T>C (p.Met201Thr)
c.557T>C (p.Met186Thr)
c.377-2514T>C (n.377-2514T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890260T>GCA350586982WNT10Ac.653T>G (p.Met218Arg)
c.264-2514T>G
c.602T>G (p.Met201Arg)
c.557T>G (p.Met186Arg)
c.377-2514T>G (n.377-2514T>G)
ClinVar dbSNP
2g.218890260T=CA1328965139WNT10Ac.653T= (p.Met218=)
c.264-2514T=
c.602T= (p.Met201=)
c.557T= (p.Met186=)
c.377-2514T= (n.377-2514T=)
2g.218890261G>ACA65916878WNT10Ac.654G>A (p.Met218Ile)
c.264-2513G>A
c.603G>A (p.Met201Ile)
c.558G>A (p.Met186Ile)
c.377-2513G>A (n.377-2513G>A)
dbSNP
2g.218890261G>CCA350586983WNT10Ac.654G>C (p.Met218Ile)
c.264-2513G>C
c.603G>C (p.Met201Ile)
c.558G>C (p.Met186Ile)
c.377-2513G>C (n.377-2513G>C)
2g.218890261G=CA1328965144WNT10Ac.654G= (p.Met218=)
c.264-2513G=
c.603G= (p.Met201=)
c.558G= (p.Met186=)
c.377-2513G= (n.377-2513G=)
2g.218890261G>TCA350586985WNT10Ac.654G>T (p.Met218Ile)
c.264-2513G>T
c.603G>T (p.Met201Ile)
c.558G>T (p.Met186Ile)
c.377-2513G>T (n.377-2513G>T)
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=)

Number of alleles fetched