Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.218890249_218890261del | CA2663174291 | WNT10A | c.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 |
2 | g.218890257A= | CA1328965128 | WNT10A | c.650A= (p.Asp217=) c.264-2517A= c.599A= (p.Asp200=) c.554A= (p.Asp185=) c.377-2517A= (n.377-2517A=) | |
2 | g.218890257A>C | CA350586944 | WNT10A | c.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) | |
2 | g.218890257A>G | CA16604387 | WNT10A | c.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 |
2 | g.218890257A>T | CA350586961 | WNT10A | c.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) | |
2 | g.218890258C>A | CA350586966 | WNT10A | c.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) | |
2 | g.218890258C>G | CA350586967 | WNT10A | c.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) | |
2 | g.218890258C>T | CA431416789 | WNT10A | c.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 |
2 | g.218890259A= | CA1328965129 | WNT10A | c.652A= (p.Met218=) c.264-2515A= c.601A= (p.Met201=) c.556A= (p.Met186=) c.377-2515A= (n.377-2515A=) | |
2 | g.218890259A>C | CA65916870 | WNT10A | c.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 |
2 | g.218890259A>G | CA2113987 | WNT10A | c.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 |
2 | g.218890259A>T | CA350586978 | WNT10A | c.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) | |
2 | g.218890260T>A | CA350586981 | WNT10A | c.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) | |
2 | g.218890260T>C | CA2113988 | WNT10A | c.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 |
2 | g.218890260T>G | CA350586982 | WNT10A | c.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 |
2 | g.218890260T= | CA1328965139 | WNT10A | c.653T= (p.Met218=) c.264-2514T= c.602T= (p.Met201=) c.557T= (p.Met186=) c.377-2514T= (n.377-2514T=) | |
2 | g.218890261G>A | CA65916878 | WNT10A | c.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 |
2 | g.218890261G>C | CA350586983 | WNT10A | c.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) | |
2 | g.218890261G= | CA1328965144 | WNT10A | c.654G= (p.Met218=) c.264-2513G= c.603G= (p.Met201=) c.558G= (p.Met186=) c.377-2513G= (n.377-2513G=) | |
2 | g.218890261G>T | CA350586985 | WNT10A | c.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) | |
2 | g.218890262G>A | CA350586994 | WNT10A | c.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) | |
2 | g.218890262G>C | CA350586997 | WNT10A | c.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) | |
2 | g.218890262G>T | CA350587004 | WNT10A | c.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) | |
2 | g.218890263G>A | CA350587011 | WNT10A | c.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 |
2 | g.218890263G>C | CA350587014 | WNT10A | c.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) | |
2 | g.218890263G= | CA1328965146 | WNT10A | c.656G= (p.Gly219=) c.264-2511G= c.605G= (p.Gly202=) c.560G= (p.Gly187=) c.377-2511G= (n.377-2511G=) | |
2 | g.218890263G>T | CA350587015 | WNT10A | c.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) | |
2 | g.218890264C>A | CA431416799 | WNT10A | c.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 |
2 | g.218890264C= | CA1328965147 | WNT10A | c.657C= (p.Gly219=) c.264-2510C= c.606C= (p.Gly202=) c.561C= (p.Gly187=) c.377-2510C= (n.377-2510C=) | |
2 | g.218890264C>G | CA431416800 | WNT10A | c.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) | |
2 | g.218890264C>T | CA431416801 | WNT10A | c.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) | |
2 | g.218890265T>A | CA350587017 | WNT10A | c.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) | |
2 | g.218890265T>C | CA350587019 | WNT10A | c.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) | |
2 | g.218890265T>G | CA350587022 | WNT10A | c.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) | |
2 | g.218890268_218890281del | CA2663174292 | WNT10A | c.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 |
2 | g.218890266T>A | CA350587027 | WNT10A | c.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) | |
2 | g.218890266T>C | CA350587030 | WNT10A | c.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 |
2 | g.218890266T>G | CA350587035 | WNT10A | c.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) | |
2 | g.218890267C>A | CA350587040 | WNT10A | c.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) | |
2 | g.218890267C= | CA1328965150 | WNT10A | c.660C= (p.Phe220=) c.264-2507C= c.609C= (p.Phe203=) c.564C= (p.Phe188=) c.377-2507C= (n.377-2507C=) | |
2 | g.218890267C>G | CA350587050 | WNT10A | c.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) | |
2 | g.218890267C>T | CA2113989 | WNT10A | c.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 |
2 | g.218890268G>A | CA2113990 | WNT10A | c.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 |
2 | g.218890268G>C | CA350587051 | WNT10A | c.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) | |
2 | g.218890268G= | CA1328965154 | WNT10A | c.661G= (p.Gly221=) c.264-2506G= c.610G= (p.Gly204=) c.565G= (p.Gly189=) c.377-2506G= (n.377-2506G=) | |
2 | g.218890268G>T | CA350587052 | WNT10A | c.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) | |
2 | g.218890271del | CA2663174293 | WNT10A | c.664del (p.Glu222SerfsTer21) c.264-2503del c.613del (p.Glu205SerfsTer21) c.568del (p.Glu190SerfsTer21) c.377-2503del (n.377-2503del) | gnomAD v4 |
2 | g.218890269G>A | CA350587055 | WNT10A | c.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) | |
2 | g.218890269G>C | CA350587057 | WNT10A | c.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) | |
2 | g.218890269G= | CA1328965157 | WNT10A | c.662G= (p.Gly221=) c.264-2505G= c.611G= (p.Gly204=) c.566G= (p.Gly189=) c.377-2505G= (n.377-2505G=) |