| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48966205_48966207del | CA2575143609 | WNT10B | c.1060_1062del (p.Asn354del) c.*342_*344del (n.*342_*344del) c.694_696del (p.Asn232del) c.*338_*340del (n.*338_*340del) | gnomAD v4 |
| 12 | g.48966206G>A | CA6544042 | WNT10B | c.1059C>T (p.His353=) c.*341C>T (n.*341C>T) c.693C>T (p.His231=) c.*337C>T (n.*337C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966206G>C | CA384671539 | WNT10B | c.1059C>G (p.His353Gln) c.*341C>G (n.*341C>G) c.693C>G (p.His231Gln) c.*337C>G (n.*337C>G) | |
| 12 | g.48966206G= | CA2034911843 | WNT10B | c.1059C= (p.His353=) c.*341C= (n.*341C=) c.693C= (p.His231=) c.*337C= (n.*337C=) | |
| 12 | g.48966206G>T | CA384671536 | WNT10B | c.1059C>A (p.His353Gln) c.*341C>A (n.*341C>A) c.693C>A (p.His231Gln) c.*337C>A (n.*337C>A) | |
| 12 | g.48966207T>A | CA384671545 | WNT10B | c.1058A>T (p.His353Leu) c.*340A>T (n.*340A>T) c.692A>T (p.His231Leu) c.*336A>T (n.*336A>T) | |
| 12 | g.48966207T>C | CA384671548 | WNT10B | c.1058A>G (p.His353Arg) c.*340A>G (n.*340A>G) c.692A>G (p.His231Arg) c.*336A>G (n.*336A>G) | gnomAD v4 |
| 12 | g.48966207T>G | CA384671551 | WNT10B | c.1058A>C (p.His353Pro) c.*340A>C (n.*340A>C) c.692A>C (p.His231Pro) c.*336A>C (n.*336A>C) | |
| 12 | g.48966208G>A | CA384671558 | WNT10B | c.1057C>T (p.His353Tyr) c.*339C>T (n.*339C>T) c.691C>T (p.His231Tyr) c.*335C>T (n.*335C>T) | gnomAD v4 |
| 12 | g.48966208G>C | CA384671560 | WNT10B | c.1057C>G (p.His353Asp) c.*339C>G (n.*339C>G) c.691C>G (p.His231Asp) c.*335C>G (n.*335C>G) | |
| 12 | g.48966208G>T | CA384671564 | WNT10B | c.1057C>A (p.His353Asn) c.*339C>A (n.*339C>A) c.691C>A (p.His231Asn) c.*335C>A (n.*335C>A) | |
| 12 | g.48966209C>A | CA479703717 | WNT10B | c.1056G>T (p.Gly352=) c.*338G>T (n.*338G>T) c.690G>T (p.Gly230=) c.*334G>T (n.*334G>T) | gnomAD v4 |
| 12 | g.48966209C>G | CA479703718 | WNT10B | c.1056G>C (p.Gly352=) c.*338G>C (n.*338G>C) c.690G>C (p.Gly230=) c.*334G>C (n.*334G>C) | |
| 12 | g.48966209C>T | CA479703719 | WNT10B | c.1056G>A (p.Gly352=) c.*338G>A (n.*338G>A) c.690G>A (p.Gly230=) c.*334G>A (n.*334G>A) | |
| 12 | g.48966210C>A | CA384671568 | WNT10B | c.1055G>T (p.Gly352Val) c.*337G>T (n.*337G>T) c.689G>T (p.Gly230Val) c.*333G>T (n.*333G>T) | |
| 12 | g.48966210C>G | CA384671570 | WNT10B | c.1055G>C (p.Gly352Ala) c.*337G>C (n.*337G>C) c.689G>C (p.Gly230Ala) c.*333G>C (n.*333G>C) | |
| 12 | g.48966210C>T | CA384671569 | WNT10B | c.1055G>A (p.Gly352Glu) c.*337G>A (n.*337G>A) c.689G>A (p.Gly230Glu) c.*333G>A (n.*333G>A) | gnomAD v4 |
| 12 | g.48966211C>A | CA384671573 | WNT10B | c.1054G>T (p.Gly352Trp) c.*336G>T (n.*336G>T) c.688G>T (p.Gly230Trp) c.*332G>T (n.*332G>T) | gnomAD v4 |
| 12 | g.48966211C>G | CA384671576 | WNT10B | c.1054G>C (p.Gly352Arg) c.*336G>C (n.*336G>C) c.688G>C (p.Gly230Arg) c.*332G>C (n.*332G>C) | |
| 12 | g.48966211C>T | CA384671577 | WNT10B | c.1054G>A (p.Gly352Arg) c.*336G>A (n.*336G>A) c.688G>A (p.Gly230Arg) c.*332G>A (n.*332G>A) | |
| 12 | g.48966212A= | CA2034911846 | WNT10B | c.1053T= (p.Arg351=) c.*335T= (n.*335T=) c.687T= (p.Arg229=) c.*331T= (n.*331T=) | |
| 12 | g.48966212A>C | CA479703722 | WNT10B | c.1053T>G (p.Arg351=) c.*335T>G (n.*335T>G) c.687T>G (p.Arg229=) c.*331T>G (n.*331T>G) | dbSNP |
| 12 | g.48966212A>G | CA479703723 | WNT10B | c.1053T>C (p.Arg351=) c.*335T>C (n.*335T>C) c.687T>C (p.Arg229=) c.*331T>C (n.*331T>C) | |
| 12 | g.48966212A>T | CA479703725 | WNT10B | c.1053T>A (p.Arg351=) c.*335T>A (n.*335T>A) c.687T>A (p.Arg229=) c.*331T>A (n.*331T>A) | |
| 12 | g.48966213C>A | CA384671578 | WNT10B | c.1052G>T (p.Arg351Leu) c.*334G>T (n.*334G>T) c.686G>T (p.Arg229Leu) c.*330G>T (n.*330G>T) | |
| 12 | g.48966213C= | CA2034911847 | WNT10B | c.1052G= (p.Arg351=) c.*334G= (n.*334G=) c.686G= (p.Arg229=) c.*330G= (n.*330G=) | |
| 12 | g.48966213C>G | CA384671579 | WNT10B | c.1052G>C (p.Arg351Pro) c.*334G>C (n.*334G>C) c.686G>C (p.Arg229Pro) c.*330G>C (n.*330G>C) | |
| 12 | g.48966213C>T | CA236626584 | WNT10B | c.1052G>A (p.Arg351His) c.*334G>A (n.*334G>A) c.686G>A (p.Arg229His) c.*330G>A (n.*330G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966214G>A | CA384671584 | WNT10B | c.1051C>T (p.Arg351Cys) c.*333C>T (n.*333C>T) c.685C>T (p.Arg229Cys) c.*329C>T (n.*329C>T) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 12 | g.48966214G>C | CA384671586 | WNT10B | c.1051C>G (p.Arg351Gly) c.*333C>G (n.*333C>G) c.685C>G (p.Arg229Gly) c.*329C>G (n.*329C>G) | |
| 12 | g.48966214G= | CA2034911848 | WNT10B | c.1051C= (p.Arg351=) c.*333C= (n.*333C=) c.685C= (p.Arg229=) c.*329C= (n.*329C=) | |
| 12 | g.48966214G>T | CA384671589 | WNT10B | c.1051C>A (p.Arg351Ser) c.*333C>A (n.*333C>A) c.685C>A (p.Arg229Ser) c.*329C>A (n.*329C>A) | |
| 12 | g.48966215G>A | CA479703728 | WNT10B | c.1050C>T (p.Gly350=) c.*332C>T (n.*332C>T) c.684C>T (p.Gly228=) c.*328C>T (n.*328C>T) | |
| 12 | g.48966215G>C | CA479703729 | WNT10B | c.1050C>G (p.Gly350=) c.*332C>G (n.*332C>G) c.684C>G (p.Gly228=) c.*328C>G (n.*328C>G) | |
| 12 | g.48966215G>T | CA479703727 | WNT10B | c.1050C>A (p.Gly350=) c.*332C>A (n.*332C>A) c.684C>A (p.Gly228=) c.*328C>A (n.*328C>A) | |
| 12 | g.48966216C>A | CA384671593 | WNT10B | c.1049G>T (p.Gly350Val) c.*331G>T (n.*331G>T) c.683G>T (p.Gly228Val) c.*327G>T (n.*327G>T) | |
| 12 | g.48966216C>G | CA384671595 | WNT10B | c.1049G>C (p.Gly350Ala) c.*331G>C (n.*331G>C) c.683G>C (p.Gly228Ala) c.*327G>C (n.*327G>C) | |
| 12 | g.48966216C>T | CA384671596 | WNT10B | c.1049G>A (p.Gly350Asp) c.*331G>A (n.*331G>A) c.683G>A (p.Gly228Asp) c.*327G>A (n.*327G>A) | |
| 12 | g.48966217C>A | CA384671599 | WNT10B | c.1048G>T (p.Gly350Cys) c.*330G>T (n.*330G>T) c.682G>T (p.Gly228Cys) c.*326G>T (n.*326G>T) | |
| 12 | g.48966217C>G | CA384671615 | WNT10B | c.1048G>C (p.Gly350Arg) c.*330G>C (n.*330G>C) c.682G>C (p.Gly228Arg) c.*326G>C (n.*326G>C) | |
| 12 | g.48966217C>T | CA384671601 | WNT10B | c.1048G>A (p.Gly350Ser) c.*330G>A (n.*330G>A) c.682G>A (p.Gly228Ser) c.*326G>A (n.*326G>A) | |
| 12 | g.48966218A>C | CA384671620 | WNT10B | c.1047T>G (p.Cys349Trp) c.*329T>G (n.*329T>G) c.681T>G (p.Cys227Trp) c.*325T>G (n.*325T>G) | |
| 12 | g.48966218A>G | CA479703738 | WNT10B | c.1047T>C (p.Cys349=) c.*329T>C (n.*329T>C) c.681T>C (p.Cys227=) c.*325T>C (n.*325T>C) | |
| 12 | g.48966218A>T | CA384671621 | WNT10B | c.1047T>A (p.Cys349Ter) c.*329T>A (n.*329T>A) c.681T>A (p.Cys227Ter) c.*325T>A (n.*325T>A) | |
| 12 | g.48966219C>A | CA384671628 | WNT10B | c.1046G>T (p.Cys349Phe) c.*328G>T (n.*328G>T) c.680G>T (p.Cys227Phe) c.*324G>T (n.*324G>T) | |
| 12 | g.48966219C>G | CA384671638 | WNT10B | c.1046G>C (p.Cys349Ser) c.*328G>C (n.*328G>C) c.680G>C (p.Cys227Ser) c.*324G>C (n.*324G>C) | |
| 12 | g.48966219C>T | CA384671642 | WNT10B | c.1046G>A (p.Cys349Tyr) c.*328G>A (n.*328G>A) c.680G>A (p.Cys227Tyr) c.*324G>A (n.*324G>A) | |
| 12 | g.48966220A= | CA2034911849 | WNT10B | c.1045T= (p.Cys349=) c.*327T= (n.*327T=) c.679T= (p.Cys227=) c.*323T= (n.*323T=) | |
| 12 | g.48966220A>C | CA384671643 | WNT10B | c.1045T>G (p.Cys349Gly) c.*327T>G (n.*327T>G) c.679T>G (p.Cys227Gly) c.*323T>G (n.*323T>G) | |
| 12 | g.48966220A>G | CA384671644 | WNT10B | c.1045T>C (p.Cys349Arg) c.*327T>C (n.*327T>C) c.679T>C (p.Cys227Arg) c.*323T>C (n.*323T>C) | dbSNP gnomAD v2 gnomAD v4 |