| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48966017_48966035dup | CA2618596047 | WNT10B | c.*62_*80dup (n.*62_*80dup) c.*514_*532dup (n.*514_*532dup) | gnomAD v4 |
| 12 | g.48966033del | CA2618596063 | WNT10B | c.*64del (n.*64del) c.*516del (n.*516del) | gnomAD v4 |
| 12 | g.48966033A>G | CA2618596066 | WNT10B | c.*62T>C (n.*62T>C) c.*514T>C (n.*514T>C) | gnomAD v4 |
| 12 | g.48966034G>T | CA2618596067 | WNT10B | c.*61C>A (n.*61C>A) c.*513C>A (n.*513C>A) | gnomAD v4 |
| 12 | g.48966035G>T | CA2618596068 | WNT10B | c.*60C>A (n.*60C>A) c.*512C>A (n.*512C>A) | gnomAD v4 |
| 12 | g.48966036G>T | CA2618596069 | WNT10B | c.*59C>A (n.*59C>A) c.*511C>A (n.*511C>A) | gnomAD v4 |
| 12 | g.48966037C>A | CA2618596070 | WNT10B | c.*58G>T (n.*58G>T) c.*510G>T (n.*510G>T) | gnomAD v4 |
| 12 | g.48966037C= | CA2034911722 | WNT10B | c.*58G= (n.*58G=) c.*510G= (n.*510G=) | |
| 12 | g.48966037C>T | CA2034911723 | WNT10B | c.*58G>A (n.*58G>A) c.*510G>A (n.*510G>A) | dbSNP gnomAD v4 |
| 12 | g.48966038T>C | CA2575143606 | WNT10B | c.*57A>G (n.*57A>G) c.*509A>G (n.*509A>G) | |
| 12 | g.48966039G>T | CA2618596071 | WNT10B | c.*56C>A (n.*56C>A) c.*508C>A (n.*508C>A) | gnomAD v4 |
| 12 | g.48966040A>G | CA2726308233 | WNT10B | c.*55T>C (n.*55T>C) c.*507T>C (n.*507T>C) | dbSNP |
| 12 | g.48966043del | CA2618596072 | WNT10B | c.*55del (n.*55del) c.*507del (n.*507del) | gnomAD v4 |
| 12 | g.48966043A>G | CA2618596073 | WNT10B | c.*52T>C (n.*52T>C) c.*504T>C (n.*504T>C) | gnomAD v4 |
| 12 | g.48966044G>T | CA2618596074 | WNT10B | c.*51C>A (n.*51C>A) c.*503C>A (n.*503C>A) | gnomAD v4 |
| 12 | g.48966045G>T | CA2618596075 | WNT10B | c.*50C>A (n.*50C>A) c.*502C>A (n.*502C>A) | gnomAD v4 |
| 12 | g.48966046C>A | CA2618596076 | WNT10B | c.*49G>T (n.*49G>T) c.*501G>T (n.*501G>T) | gnomAD v4 |
| 12 | g.48966046C= | CA2034911725 | WNT10B | c.*49G= (n.*49G=) c.*501G= (n.*501G=) | |
| 12 | g.48966046C>T | CA6544017 | WNT10B | c.*49G>A (n.*49G>A) c.*501G>A (n.*501G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966047G>A | CA6544018 | WNT10B | c.*48C>T (n.*48C>T) c.*500C>T (n.*500C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966047G>C | CA2618596077 | WNT10B | c.*48C>G (n.*48C>G) c.*500C>G (n.*500C>G) | gnomAD v4 |
| 12 | g.48966047G= | CA2034911727 | WNT10B | c.*48C= (n.*48C=) c.*500C= (n.*500C=) | |
| 12 | g.48966047G>T | CA2618596078 | WNT10B | c.*48C>A (n.*48C>A) c.*500C>A (n.*500C>A) | gnomAD v4 |
| 12 | g.48966048C>T | CA2618596079 | WNT10B | c.*47G>A (n.*47G>A) c.*499G>A (n.*499G>A) | gnomAD v4 |
| 12 | g.48966051del | CA2575143607 | WNT10B | c.*47del (n.*47del) c.*499del (n.*499del) | |
| 12 | g.48966049C>A | CA947437880 | WNT10B | c.*46G>T (n.*46G>T) c.*498G>T (n.*498G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48966049C= | CA2034911728 | WNT10B | c.*46G= (n.*46G=) c.*498G= (n.*498G=) | |
| 12 | g.48966049C>T | CA2618596080 | WNT10B | c.*46G>A (n.*46G>A) c.*498G>A (n.*498G>A) | gnomAD v4 |
| 12 | g.48966050C>G | CA2618596081 | WNT10B | c.*45G>C (n.*45G>C) c.*497G>C (n.*497G>C) | gnomAD v4 |
| 12 | g.48966051C>T | CA2618596082 | WNT10B | c.*44G>A (n.*44G>A) c.*496G>A (n.*496G>A) | gnomAD v4 |
| 12 | g.48966054T>C | CA689532864 | WNT10B | c.*41A>G (n.*41A>G) c.*493A>G (n.*493A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48966054T= | CA2034911731 | WNT10B | c.*41A= (n.*41A=) c.*493A= (n.*493A=) | |
| 12 | g.48966054_48966055delinsTC | CA2034911730 | WNT10B | c.*40_*41delinsGA (n.*40_*41delinsGA) c.*492_*493delinsGA (n.*492_*493delinsGA) | |
| 12 | g.48966055del | CA2034911732 | WNT10B | c.*40del (n.*40del) c.*492del (n.*492del) | dbSNP |
| 12 | g.48966055C>A | CA2618596084 | WNT10B | c.*40G>T (n.*40G>T) c.*492G>T (n.*492G>T) | gnomAD v4 |
| 12 | g.48966055C>G | CA2618596083 | WNT10B | c.*40G>C (n.*40G>C) c.*492G>C (n.*492G>C) | gnomAD v4 |
| 12 | g.48966056A= | CA2034911733 | WNT10B | c.*39T= (n.*39T=) c.*491T= (n.*491T=) | |
| 12 | g.48966056A>T | CA947437883 | WNT10B | c.*39T>A (n.*39T>A) c.*491T>A (n.*491T>A) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48966059C>T | CA2618596085 | WNT10B | c.*36G>A (n.*36G>A) c.*488G>A (n.*488G>A) | gnomAD v4 |
| 12 | g.48966060A= | CA2034911734 | WNT10B | c.*35T= (n.*35T=) c.*487T= (n.*487T=) | |
| 12 | g.48966060A>C | CA2034911735 | WNT10B | c.*35T>G (n.*35T>G) c.*487T>G (n.*487T>G) | dbSNP |
| 12 | g.48966060A>G | CA2618596086 | WNT10B | c.*35T>C (n.*35T>C) c.*487T>C (n.*487T>C) | gnomAD v4 |
| 12 | g.48966061G>A | CA2618596087 | WNT10B | c.*34C>T (n.*34C>T) c.*486C>T (n.*486C>T) | gnomAD v4 |
| 12 | g.48966061G>T | CA2618596088 | WNT10B | c.*34C>A (n.*34C>A) c.*486C>A (n.*486C>A) | gnomAD v4 |
| 12 | g.48966063C= | CA2034911736 | WNT10B | c.*32G= (n.*32G=) c.*484G= (n.*484G=) | |
| 12 | g.48966063C>G | CA2034911738 | WNT10B | c.*32G>C (n.*32G>C) c.*484G>C (n.*484G>C) | dbSNP gnomAD v4 |
| 12 | g.48966063C>T | CA2618596089 | WNT10B | c.*32G>A (n.*32G>A) c.*484G>A (n.*484G>A) | gnomAD v4 |
| 12 | g.48966064C= | CA2034911739 | WNT10B | c.*31G= (n.*31G=) c.*483G= (n.*483G=) | |
| 12 | g.48966064C>T | CA2034911740 | WNT10B | c.*31G>A (n.*31G>A) c.*483G>A (n.*483G>A) | dbSNP |
| 12 | g.48966066_48966067insG | CA654731926 | WNT10B | c.*28_*29insC (n.*28_*29insC) c.*480_*481insC (n.*480_*481insC) | COSMIC |
| 12 | g.48966067T>C | CA605233217 | WNT10B | c.*28A>G (n.*28A>G) c.*480A>G (n.*480A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48966067T= | CA2034911741 | WNT10B | c.*28A= (n.*28A=) c.*480A= (n.*480A=) | |
| 12 | g.48966068T>C | CA2506928263 | WNT10B | c.*27A>G (n.*27A>G) c.*479A>G (n.*479A>G) | |
| 12 | g.48966069C>A | CA6544019 | WNT10B | c.*26G>T (n.*26G>T) c.*478G>T (n.*478G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966069C= | CA2034911744 | WNT10B | c.*26G= (n.*26G=) c.*478G= (n.*478G=) | |
| 12 | g.48966069C>T | CA2034911743 | WNT10B | c.*26G>A (n.*26G>A) c.*478G>A (n.*478G>A) | dbSNP gnomAD v4 |
| 12 | g.48966070C>A | CA2034911747 | WNT10B | c.*25G>T (n.*25G>T) c.*477G>T (n.*477G>T) | dbSNP gnomAD v4 |
| 12 | g.48966070C= | CA2034911745 | WNT10B | c.*25G= (n.*25G=) c.*477G= (n.*477G=) | |
| 12 | g.48966070C>T | CA605233218 | WNT10B | c.*25G>A (n.*25G>A) c.*477G>A (n.*477G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966071C>A | CA2618596090 | WNT10B | c.*24G>T (n.*24G>T) c.*476G>T (n.*476G>T) | gnomAD v4 |
| 12 | g.48966073A= | CA2034911748 | WNT10B | c.*22T= (n.*22T=) c.*474T= (n.*474T=) | |
| 12 | g.48966073A>G | CA6544020 | WNT10B | c.*22T>C (n.*22T>C) c.*474T>C (n.*474T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966074G>A | CA2575143608 | WNT10B | c.*21C>T (n.*21C>T) c.*473C>T (n.*473C>T) | |
| 12 | g.48966074G>T | CA2618596091 | WNT10B | c.*21C>A (n.*21C>A) c.*473C>A (n.*473C>A) | gnomAD v4 |
| 12 | g.48966075C>A | CA2618596092 | WNT10B | c.*20G>T (n.*20G>T) c.*472G>T (n.*472G>T) | gnomAD v4 |
| 12 | g.48966075C= | CA2034911750 | WNT10B | c.*20G= (n.*20G=) c.*472G= (n.*472G=) | |
| 12 | g.48966075C>T | CA605233219 | WNT10B | c.*20G>A (n.*20G>A) c.*472G>A (n.*472G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48966078del | CA2618596093 | WNT10B | c.*20del (n.*20del) c.*472del (n.*472del) | gnomAD v4 |
| 12 | g.48966077C>A | CA6544021 | WNT10B | c.*18G>T (n.*18G>T) c.*470G>T (n.*470G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966077C= | CA2034911751 | WNT10B | c.*18G= (n.*18G=) c.*470G= (n.*470G=) | |
| 12 | g.48966077C>G | CA2618596094 | WNT10B | c.*18G>C (n.*18G>C) c.*470G>C (n.*470G>C) | gnomAD v4 |
| 12 | g.48966077C>T | CA2618596095 | WNT10B | c.*18G>A (n.*18G>A) c.*470G>A (n.*470G>A) | gnomAD v4 |
| 12 | g.48966078C>A | CA2526390634 | WNT10B | c.*17G>T (n.*17G>T) c.*469G>T (n.*469G>T) | |
| 12 | g.48966078C>T | CA2618596096 | WNT10B | c.*17G>A (n.*17G>A) c.*469G>A (n.*469G>A) | gnomAD v4 |
| 12 | g.48966080A= | CA2034911752 | WNT10B | c.*15T= (n.*15T=) c.*467T= (n.*467T=) | |
| 12 | g.48966080A>G | CA605233220 | WNT10B | c.*15T>C (n.*15T>C) c.*467T>C (n.*467T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48966080A>T | CA2618596097 | WNT10B | c.*15T>A (n.*15T>A) c.*467T>A (n.*467T>A) | gnomAD v4 |
| 12 | g.48966081G>A | CA2034911755 | WNT10B | c.*14C>T (n.*14C>T) c.*466C>T (n.*466C>T) | dbSNP |
| 12 | g.48966081G= | CA2034911754 | WNT10B | c.*14C= (n.*14C=) c.*466C= (n.*466C=) | |
| 12 | g.48966082G>A | CA2618596098 | WNT10B | c.*13C>T (n.*13C>T) c.*465C>T (n.*465C>T) | gnomAD v4 |
| 12 | g.48966082G>C | CA2618596099 | WNT10B | c.*13C>G (n.*13C>G) c.*465C>G (n.*465C>G) | gnomAD v4 |
| 12 | g.48966082G>T | CA2596225406 | WNT10B | c.*13C>A (n.*13C>A) c.*465C>A (n.*465C>A) | gnomAD v3 gnomAD v4 |
| 12 | g.48966087G>A | CA2618596100 | WNT10B | c.*8C>T (n.*8C>T) c.*460C>T (n.*460C>T) | gnomAD v4 |
| 12 | g.48966087G>C | CA2034911757 | WNT10B | c.*8C>G (n.*8C>G) c.*460C>G (n.*460C>G) | dbSNP |
| 12 | g.48966087G= | CA2034911756 | WNT10B | c.*8C= (n.*8C=) c.*460C= (n.*460C=) | |
| 12 | g.48966087G>T | CA2618596101 | WNT10B | c.*8C>A (n.*8C>A) c.*460C>A (n.*460C>A) | gnomAD v4 |
| 12 | g.48966091A= | CA2034911758 | WNT10B | c.*4T= (n.*4T=) c.*456T= (n.*456T=) | |
| 12 | g.48966091A>G | CA6544022 | WNT10B | c.*4T>C (n.*4T>C) c.*456T>C (n.*456T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966092C= | CA2034911760 | WNT10B | c.*3G= (n.*3G=) c.*455G= (n.*455G=) | |
| 12 | g.48966092C>T | CA605233222 | WNT10B | c.*3G>A (n.*3G>A) c.*455G>A (n.*455G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48966094dup | CA605233221 | WNT10B | c.*3dup (n.*3dup) c.*455dup (n.*455dup) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48966093C>T | CA2618596102 | WNT10B | c.*2G>A (n.*2G>A) c.*454G>A (n.*454G>A) | gnomAD v4 |
| 12 | g.48966094C>T | CA2795900369 | WNT10B | c.*1G>A (n.*1G>A) c.*453G>A (n.*453G>A) | |
| 12 | g.48966095T>A | CA384670637 | WNT10B | c.1170A>T (p.Ter390Cys) c.*452A>T (n.*452A>T) c.804A>T (p.Ter268Cys) | |
| 12 | g.48966095T>C | CA384670634 | WNT10B | c.1170A>G (p.Ter390Trp) c.*452A>G (n.*452A>G) c.804A>G (p.Ter268Trp) | |
| 12 | g.48966095T>G | CA384670646 | WNT10B | c.1170A>C (p.Ter390Cys) c.*452A>C (n.*452A>C) c.804A>C (p.Ter268Cys) | gnomAD v4 |
| 12 | g.48966096C>A | CA384670651 | WNT10B | c.1169G>T (p.Ter390Leu) c.*451G>T (n.*451G>T) c.803G>T (p.Ter268Leu) | |
| 12 | g.48966096C= | CA2034911763 | WNT10B | c.1169G= (p.Ter390=) c.*451G= (n.*451G=) c.803G= (p.Ter268=) | |
| 12 | g.48966096C>G | CA384670654 | WNT10B | c.1169G>C (p.Ter390Ser) c.*451G>C (n.*451G>C) c.803G>C (p.Ter268Ser) | |
| 12 | g.48966096C>T | CA479703436 | WNT10B | c.1169G>A (p.Ter390=) c.*451G>A (n.*451G>A) c.803G>A (p.Ter268=) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48966096_48966100delinsCACTT | CA2034911762 | WNT10B | c.1165_1169delinsAAGTG (p.Lys389=) c.*447_*451delinsAAGTG (n.*447_*451delinsAAGTG) c.799_803delinsAAGTG (p.Lys267=) | |
| 12 | g.48966097A= | CA2034911765 | WNT10B | c.1168T= (p.Ter390=) c.*450T= (n.*450T=) c.802T= (p.Ter268=) | |
| 12 | g.48966097A>C | CA6544024 | WNT10B | c.1168T>G (p.Ter390Gly) c.*450T>G (n.*450T>G) c.802T>G (p.Ter268Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966097A>G | CA384670664 | WNT10B | c.1168T>C (p.Ter390Arg) c.*450T>C (n.*450T>C) c.802T>C (p.Ter268Arg) | |
| 12 | g.48966097A>T | CA384670666 | WNT10B | c.1168T>A (p.Ter390Arg) c.*450T>A (n.*450T>A) c.802T>A (p.Ter268Arg) | |
| 12 | g.48966099_48966102del | CA6544023 | WNT10B | c.1165_1168del (p.Lys389GlufsTer?) c.*447_*450del (n.*447_*450del) c.799_802del (p.Lys267GlufsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966098C>A | CA384670670 | WNT10B | c.1167G>T (p.Lys389Asn) c.*449G>T (n.*449G>T) c.801G>T (p.Lys267Asn) | |
| 12 | g.48966098C= | CA2034911766 | WNT10B | c.1167G= (p.Lys389=) c.*449G= (n.*449G=) c.801G= (p.Lys267=) | |
| 12 | g.48966098C>G | CA236626505 | WNT10B | c.1167G>C (p.Lys389Asn) c.*449G>C (n.*449G>C) c.801G>C (p.Lys267Asn) | dbSNP gnomAD v2 |
| 12 | g.48966098C>T | CA479703438 | WNT10B | c.1167G>A (p.Lys389=) c.*449G>A (n.*449G>A) c.801G>A (p.Lys267=) | gnomAD v4 |
| 12 | g.48966099T>A | CA384670676 | WNT10B | c.1166A>T (p.Lys389Met) c.*448A>T (n.*448A>T) c.800A>T (p.Lys267Met) | |
| 12 | g.48966099T>C | CA384670679 | WNT10B | c.1166A>G (p.Lys389Arg) c.*448A>G (n.*448A>G) c.800A>G (p.Lys267Arg) | COSMIC |
| 12 | g.48966099T>G | CA384670683 | WNT10B | c.1166A>C (p.Lys389Thr) c.*448A>C (n.*448A>C) c.800A>C (p.Lys267Thr) | |
| 12 | g.48966100T>A | CA384670687 | WNT10B | c.1165A>T (p.Lys389Ter) c.*447A>T (n.*447A>T) c.799A>T (p.Lys267Ter) | |
| 12 | g.48966100T>C | CA384670690 | WNT10B | c.1165A>G (p.Lys389Glu) c.*447A>G (n.*447A>G) c.799A>G (p.Lys267Glu) | |
| 12 | g.48966100T>G | CA384670693 | WNT10B | c.1165A>C (p.Lys389Gln) c.*447A>C (n.*447A>C) c.799A>C (p.Lys267Gln) | |
| 12 | g.48966101A>C | CA384670696 | WNT10B | c.1164T>G (p.Cys388Trp) c.*446T>G (n.*446T>G) c.798T>G (p.Cys266Trp) | |
| 12 | g.48966101A>G | CA479703441 | WNT10B | c.1164T>C (p.Cys388=) c.*446T>C (n.*446T>C) c.798T>C (p.Cys266=) | |
| 12 | g.48966101A>T | CA384670698 | WNT10B | c.1164T>A (p.Cys388Ter) c.*446T>A (n.*446T>A) c.798T>A (p.Cys266Ter) | |
| 12 | g.48966102C>A | CA384670709 | WNT10B | c.1163G>T (p.Cys388Phe) c.*445G>T (n.*445G>T) c.797G>T (p.Cys266Phe) | |
| 12 | g.48966102C>G | CA384670706 | WNT10B | c.1163G>C (p.Cys388Ser) c.*445G>C (n.*445G>C) c.797G>C (p.Cys266Ser) | |
| 12 | g.48966102C>T | CA384670702 | WNT10B | c.1163G>A (p.Cys388Tyr) c.*445G>A (n.*445G>A) c.797G>A (p.Cys266Tyr) | |
| 12 | g.48966103A= | CA2034911768 | WNT10B | c.1162T= (p.Cys388=) c.*444T= (n.*444T=) c.796T= (p.Cys266=) | |
| 12 | g.48966103A>C | CA384670713 | WNT10B | c.1162T>G (p.Cys388Gly) c.*444T>G (n.*444T>G) c.796T>G (p.Cys266Gly) | |
| 12 | g.48966103A>G | CA384670714 | WNT10B | c.1162T>C (p.Cys388Arg) c.*444T>C (n.*444T>C) c.796T>C (p.Cys266Arg) | dbSNP |
| 12 | g.48966103A>T | CA384670717 | WNT10B | c.1162T>A (p.Cys388Ser) c.*444T>A (n.*444T>A) c.796T>A (p.Cys266Ser) | |
| 12 | g.48966104C>A | CA479703446 | WNT10B | c.1161G>T (p.Val387=) c.*443G>T (n.*443G>T) c.795G>T (p.Val265=) | |
| 12 | g.48966104C= | CA2034911770 | WNT10B | c.1161G= (p.Val387=) c.*443G= (n.*443G=) c.795G= (p.Val265=) | |
| 12 | g.48966104C>G | CA479703448 | WNT10B | c.1161G>C (p.Val387=) c.*443G>C (n.*443G>C) c.795G>C (p.Val265=) | dbSNP |
| 12 | g.48966104C>T | CA479703447 | WNT10B | c.1161G>A (p.Val387=) c.*443G>A (n.*443G>A) c.795G>A (p.Val265=) | dbSNP |
| 12 | g.48966105del | CA2618596103 | WNT10B | c.1160del (p.Val387GlyfsTer?) c.*442del (n.*442del) c.794del (p.Val265GlyfsTer?) | gnomAD v4 |
| 12 | g.48966105A>C | CA384670722 | WNT10B | c.1160T>G (p.Val387Gly) c.*442T>G (n.*442T>G) c.794T>G (p.Val265Gly) | |
| 12 | g.48966105A>G | CA384670724 | WNT10B | c.1160T>C (p.Val387Ala) c.*442T>C (n.*442T>C) c.794T>C (p.Val265Ala) | |
| 12 | g.48966105A>T | CA384670727 | WNT10B | c.1160T>A (p.Val387Glu) c.*442T>A (n.*442T>A) c.794T>A (p.Val265Glu) | |
| 12 | g.48966106C>A | CA384670731 | WNT10B | c.1159G>T (p.Val387Leu) c.*441G>T (n.*441G>T) c.793G>T (p.Val265Leu) | |
| 12 | g.48966106C>G | CA384670734 | WNT10B | c.1159G>C (p.Val387Leu) c.*441G>C (n.*441G>C) c.793G>C (p.Val265Leu) | |
| 12 | g.48966106C>T | CA384670738 | WNT10B | c.1159G>A (p.Val387Met) c.*441G>A (n.*441G>A) c.793G>A (p.Val265Met) | |
| 12 | g.48966107A>C | CA384670741 | WNT10B | c.1158T>G (p.Asn386Lys) c.*440T>G (n.*440T>G) c.792T>G (p.Asn264Lys) | |
| 12 | g.48966107A>G | CA479703451 | WNT10B | c.1158T>C (p.Asn386=) c.*440T>C (n.*440T>C) c.792T>C (p.Asn264=) | dbSNP |
| 12 | g.48966107A>T | CA384670744 | WNT10B | c.1158T>A (p.Asn386Lys) c.*440T>A (n.*440T>A) c.792T>A (p.Asn264Lys) | |
| 12 | g.48966108T>A | CA384670754 | WNT10B | c.1157A>T (p.Asn386Ile) c.*439A>T (n.*439A>T) c.791A>T (p.Asn264Ile) | dbSNP |
| 12 | g.48966108T>C | CA384670751 | WNT10B | c.1157A>G (p.Asn386Ser) c.*439A>G (n.*439A>G) c.791A>G (p.Asn264Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966108T>G | CA384670748 | WNT10B | c.1157A>C (p.Asn386Thr) c.*439A>C (n.*439A>C) c.791A>C (p.Asn264Thr) | |
| 12 | g.48966108T= | CA2034911772 | WNT10B | c.1157A= (p.Asn386=) c.*439A= (n.*439A=) c.791A= (p.Asn264=) | |
| 12 | g.48966109T>A | CA384670757 | WNT10B | c.1156A>T (p.Asn386Tyr) c.*438A>T (n.*438A>T) c.790A>T (p.Asn264Tyr) | |
| 12 | g.48966109T>C | CA384670759 | WNT10B | c.1156A>G (p.Asn386Asp) c.*438A>G (n.*438A>G) c.790A>G (p.Asn264Asp) | |
| 12 | g.48966109T>G | CA384670762 | WNT10B | c.1156A>C (p.Asn386His) c.*438A>C (n.*438A>C) c.790A>C (p.Asn264His) | |
| 12 | g.48966110C>A | CA479703455 | WNT10B | c.1155G>T (p.Val385=) c.*437G>T (n.*437G>T) c.789G>T (p.Val263=) | |
| 12 | g.48966110C= | CA2034911774 | WNT10B | c.1155G= (p.Val385=) c.*437G= (n.*437G=) c.789G= (p.Val263=) | |
| 12 | g.48966110C>G | CA6544026 | WNT10B | c.1155G>C (p.Val385=) c.*437G>C (n.*437G>C) c.789G>C (p.Val263=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966110C>T | CA6544025 | WNT10B | c.1155G>A (p.Val385=) c.*437G>A (n.*437G>A) c.789G>A (p.Val263=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966111del | CA2795900370 | WNT10B | c.1154del (p.Val385GlyfsTer?) c.*436del (n.*436del) c.788del (p.Val263GlyfsTer?) | |
| 12 | g.48966111A>C | CA384670779 | WNT10B | c.1154T>G (p.Val385Gly) c.*436T>G (n.*436T>G) c.788T>G (p.Val263Gly) | |
| 12 | g.48966111A>G | CA384670776 | WNT10B | c.1154T>C (p.Val385Ala) c.*436T>C (n.*436T>C) c.788T>C (p.Val263Ala) | |
| 12 | g.48966111A>T | CA384670772 | WNT10B | c.1154T>A (p.Val385Glu) c.*436T>A (n.*436T>A) c.788T>A (p.Val263Glu) | |
| 12 | g.48966112C>A | CA384670781 | WNT10B | c.1153G>T (p.Val385Leu) c.*435G>T (n.*435G>T) c.787G>T (p.Val263Leu) | |
| 12 | g.48966112C>G | CA384670784 | WNT10B | c.1153G>C (p.Val385Leu) c.*435G>C (n.*435G>C) c.787G>C (p.Val263Leu) | |
| 12 | g.48966112C>T | CA384670788 | WNT10B | c.1153G>A (p.Val385Met) c.*435G>A (n.*435G>A) c.787G>A (p.Val263Met) | gnomAD v4 |
| 12 | g.48966113C>A | CA384670792 | WNT10B | c.1152G>T (p.Trp384Cys) c.*434G>T (n.*434G>T) c.786G>T (p.Trp262Cys) | |
| 12 | g.48966113C= | CA2034911777 | WNT10B | c.1152G= (p.Trp384=) c.*434G= (n.*434G=) c.786G= (p.Trp262=) | |
| 12 | g.48966113C>G | CA384670795 | WNT10B | c.1152G>C (p.Trp384Cys) c.*434G>C (n.*434G>C) c.786G>C (p.Trp262Cys) | dbSNP gnomAD v4 |
| 12 | g.48966113C>T | CA384670797 | WNT10B | c.1152G>A (p.Trp384Ter) c.*434G>A (n.*434G>A) c.786G>A (p.Trp262Ter) | |
| 12 | g.48966114C>A | CA384670802 | WNT10B | c.1151G>T (p.Trp384Leu) c.*433G>T (n.*433G>T) c.785G>T (p.Trp262Leu) | |
| 12 | g.48966114C= | CA2034911778 | WNT10B | c.1151G= (p.Trp384=) c.*433G= (n.*433G=) c.785G= (p.Trp262=) | |
| 12 | g.48966114C>G | CA384670808 | WNT10B | c.1151G>C (p.Trp384Ser) c.*433G>C (n.*433G>C) c.785G>C (p.Trp262Ser) | |
| 12 | g.48966114C>T | CA384670806 | WNT10B | c.1151G>A (p.Trp384Ter) c.*433G>A (n.*433G>A) c.785G>A (p.Trp262Ter) | dbSNP gnomAD v4 COSMIC |
| 12 | g.48966115A>C | CA384670812 | WNT10B | c.1150T>G (p.Trp384Gly) c.*432T>G (n.*432T>G) c.784T>G (p.Trp262Gly) | |
| 12 | g.48966115A>G | CA384670814 | WNT10B | c.1150T>C (p.Trp384Arg) c.*432T>C (n.*432T>C) c.784T>C (p.Trp262Arg) | gnomAD v4 |
| 12 | g.48966115A>T | CA384670816 | WNT10B | c.1150T>A (p.Trp384Arg) c.*432T>A (n.*432T>A) c.784T>A (p.Trp262Arg) | |
| 12 | g.48966116C>A | CA384670819 | WNT10B | c.1149G>T (p.Glu383Asp) c.*431G>T (n.*431G>T) c.783G>T (p.Glu261Asp) | |
| 12 | g.48966116C>G | CA384670820 | WNT10B | c.1149G>C (p.Glu383Asp) c.*431G>C (n.*431G>C) c.783G>C (p.Glu261Asp) | |
| 12 | g.48966116C>T | CA479703460 | WNT10B | c.1149G>A (p.Glu383=) c.*431G>A (n.*431G>A) c.783G>A (p.Glu261=) | |
| 12 | g.48966117T>A | CA384670824 | WNT10B | c.1148A>T (p.Glu383Val) c.*430A>T (n.*430A>T) c.782A>T (p.Glu261Val) | |
| 12 | g.48966117T>C | CA6544027 | WNT10B | c.1148A>G (p.Glu383Gly) c.*430A>G (n.*430A>G) c.782A>G (p.Glu261Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966117T>G | CA384670830 | WNT10B | c.1148A>C (p.Glu383Ala) c.*430A>C (n.*430A>C) c.782A>C (p.Glu261Ala) | |
| 12 | g.48966117T= | CA2034911780 | WNT10B | c.1148A= (p.Glu383=) c.*430A= (n.*430A=) c.782A= (p.Glu261=) | |
| 12 | g.48966118C>A | CA384670834 | WNT10B | c.1147G>T (p.Glu383Ter) c.*429G>T (n.*429G>T) c.781G>T (p.Glu261Ter) | |
| 12 | g.48966118C>G | CA384670837 | WNT10B | c.1147G>C (p.Glu383Gln) c.*429G>C (n.*429G>C) c.781G>C (p.Glu261Gln) | |
| 12 | g.48966118C>T | CA384670840 | WNT10B | c.1147G>A (p.Glu383Lys) c.*429G>A (n.*429G>A) c.781G>A (p.Glu261Lys) | |
| 12 | g.48966119T>A | CA479703462 | WNT10B | c.1146A>T (p.Thr382=) c.*428A>T (n.*428A>T) c.780A>T (p.Thr260=) c.*424A>T (n.*424A>T) | |
| 12 | g.48966119T>C | CA6544028 | WNT10B | c.1146A>G (p.Thr382=) c.*428A>G (n.*428A>G) c.780A>G (p.Thr260=) c.*424A>G (n.*424A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966119T>G | CA479703461 | WNT10B | c.1146A>C (p.Thr382=) c.*428A>C (n.*428A>C) c.780A>C (p.Thr260=) c.*424A>C (n.*424A>C) | |
| 12 | g.48966119T= | CA2034911782 | WNT10B | c.1146A= (p.Thr382=) c.*428A= (n.*428A=) c.780A= (p.Thr260=) c.*424A= (n.*424A=) | |
| 12 | g.48966120G>A | CA384670850 | WNT10B | c.1145C>T (p.Thr382Ile) c.*427C>T (n.*427C>T) c.779C>T (p.Thr260Ile) c.*423C>T (n.*423C>T) | |
| 12 | g.48966120G>C | CA384670847 | WNT10B | c.1145C>G (p.Thr382Arg) c.*427C>G (n.*427C>G) c.779C>G (p.Thr260Arg) c.*423C>G (n.*423C>G) | |
| 12 | g.48966120G>T | CA384670848 | WNT10B | c.1145C>A (p.Thr382Lys) c.*427C>A (n.*427C>A) c.779C>A (p.Thr260Lys) c.*423C>A (n.*423C>A) | |
| 12 | g.48966121T>A | CA384670854 | WNT10B | c.1144A>T (p.Thr382Ser) c.*426A>T (n.*426A>T) c.778A>T (p.Thr260Ser) c.*422A>T (n.*422A>T) | |
| 12 | g.48966121T>C | CA384670856 | WNT10B | c.1144A>G (p.Thr382Ala) c.*426A>G (n.*426A>G) c.778A>G (p.Thr260Ala) c.*422A>G (n.*422A>G) | |
| 12 | g.48966121T>G | CA384670858 | WNT10B | c.1144A>C (p.Thr382Pro) c.*426A>C (n.*426A>C) c.778A>C (p.Thr260Pro) c.*422A>C (n.*422A>C) | |
| 12 | g.48966122A>C | CA479703463 | WNT10B | c.1143T>G (p.Val381=) c.*425T>G (n.*425T>G) c.777T>G (p.Val259=) c.*421T>G (n.*421T>G) | |
| 12 | g.48966122A>G | CA479703464 | WNT10B | c.1143T>C (p.Val381=) c.*425T>C (n.*425T>C) c.777T>C (p.Val259=) c.*421T>C (n.*421T>C) | |
| 12 | g.48966122A>T | CA479703465 | WNT10B | c.1143T>A (p.Val381=) c.*425T>A (n.*425T>A) c.777T>A (p.Val259=) c.*421T>A (n.*421T>A) | |
| 12 | g.48966123A>C | CA384670863 | WNT10B | c.1142T>G (p.Val381Gly) c.*424T>G (n.*424T>G) c.776T>G (p.Val259Gly) c.*420T>G (n.*420T>G) | |
| 12 | g.48966123A>G | CA384670866 | WNT10B | c.1142T>C (p.Val381Ala) c.*424T>C (n.*424T>C) c.776T>C (p.Val259Ala) c.*420T>C (n.*420T>C) | |
| 12 | g.48966123A>T | CA384670868 | WNT10B | c.1142T>A (p.Val381Asp) c.*424T>A (n.*424T>A) c.776T>A (p.Val259Asp) c.*420T>A (n.*420T>A) | |
| 12 | g.48966124C>A | CA384670872 | WNT10B | c.1141G>T (p.Val381Phe) c.*423G>T (n.*423G>T) c.775G>T (p.Val259Phe) c.*419G>T (n.*419G>T) | dbSNP |
| 12 | g.48966124C= | CA2034911783 | WNT10B | c.1141G= (p.Val381=) c.*423G= (n.*423G=) c.775G= (p.Val259=) c.*419G= (n.*419G=) | |
| 12 | g.48966124C>G | CA384670874 | WNT10B | c.1141G>C (p.Val381Leu) c.*423G>C (n.*423G>C) c.775G>C (p.Val259Leu) c.*419G>C (n.*419G>C) | |
| 12 | g.48966124C>T | CA384670876 | WNT10B | c.1141G>A (p.Val381Ile) c.*423G>A (n.*423G>A) c.775G>A (p.Val259Ile) c.*419G>A (n.*419G>A) | COSMIC |
| 12 | g.48966125C>A | CA384670877 | WNT10B | c.1140G>T (p.Lys380Asn) c.*422G>T (n.*422G>T) c.774G>T (p.Lys258Asn) c.*418G>T (n.*418G>T) | |
| 12 | g.48966125C>G | CA384670878 | WNT10B | c.1140G>C (p.Lys380Asn) c.*422G>C (n.*422G>C) c.774G>C (p.Lys258Asn) c.*418G>C (n.*418G>C) | gnomAD v4 |
| 12 | g.48966125C>T | CA479703466 | WNT10B | c.1140G>A (p.Lys380=) c.*422G>A (n.*422G>A) c.774G>A (p.Lys258=) c.*418G>A (n.*418G>A) | gnomAD v4 |
| 12 | g.48966126T>A | CA384670882 | WNT10B | c.1139A>T (p.Lys380Met) c.*421A>T (n.*421A>T) c.773A>T (p.Lys258Met) c.*417A>T (n.*417A>T) | |
| 12 | g.48966126T>C | CA384670881 | WNT10B | c.1139A>G (p.Lys380Arg) c.*421A>G (n.*421A>G) c.773A>G (p.Lys258Arg) c.*417A>G (n.*417A>G) | |
| 12 | g.48966126T>G | CA384670879 | WNT10B | c.1139A>C (p.Lys380Thr) c.*421A>C (n.*421A>C) c.773A>C (p.Lys258Thr) c.*417A>C (n.*417A>C) | |
| 12 | g.48966127T>A | CA384670885 | WNT10B | c.1138A>T (p.Lys380Ter) c.*420A>T (n.*420A>T) c.772A>T (p.Lys258Ter) c.*416A>T (n.*416A>T) | |
| 12 | g.48966127T>C | CA384670887 | WNT10B | c.1138A>G (p.Lys380Glu) c.*420A>G (n.*420A>G) c.772A>G (p.Lys258Glu) c.*416A>G (n.*416A>G) | |
| 12 | g.48966127T>G | CA384670890 | WNT10B | c.1138A>C (p.Lys380Gln) c.*420A>C (n.*420A>C) c.772A>C (p.Lys258Gln) c.*416A>C (n.*416A>C) | |
| 12 | g.48966128G>A | CA479703597 | WNT10B | c.1137C>T (p.Cys379=) c.*419C>T (n.*419C>T) c.771C>T (p.Cys257=) c.*415C>T (n.*415C>T) | |
| 12 | g.48966128G>C | CA384670894 | WNT10B | c.1137C>G (p.Cys379Trp) c.*419C>G (n.*419C>G) c.771C>G (p.Cys257Trp) c.*415C>G (n.*415C>G) | |
| 12 | g.48966128G>T | CA384670897 | WNT10B | c.1137C>A (p.Cys379Ter) c.*419C>A (n.*419C>A) c.771C>A (p.Cys257Ter) c.*415C>A (n.*415C>A) | |
| 12 | g.48966129C>A | CA384670900 | WNT10B | c.1136G>T (p.Cys379Phe) c.*418G>T (n.*418G>T) c.770G>T (p.Cys257Phe) c.*414G>T (n.*414G>T) | |
| 12 | g.48966129C= | CA2034911785 | WNT10B | c.1136G= (p.Cys379=) c.*418G= (n.*418G=) c.770G= (p.Cys257=) c.*414G= (n.*414G=) | |
| 12 | g.48966129C>G | CA384670902 | WNT10B | c.1136G>C (p.Cys379Ser) c.*418G>C (n.*418G>C) c.770G>C (p.Cys257Ser) c.*414G>C (n.*414G>C) | |
| 12 | g.48966129C>T | CA236626515 | WNT10B | c.1136G>A (p.Cys379Tyr) c.*418G>A (n.*418G>A) c.770G>A (p.Cys257Tyr) c.*414G>A (n.*414G>A) | dbSNP gnomAD v4 |
| 12 | g.48966130A>C | CA384670909 | WNT10B | c.1135T>G (p.Cys379Gly) c.*417T>G (n.*417T>G) c.769T>G (p.Cys257Gly) c.*413T>G (n.*413T>G) | |
| 12 | g.48966130A>G | CA384670910 | WNT10B | c.1135T>C (p.Cys379Arg) c.*417T>C (n.*417T>C) c.769T>C (p.Cys257Arg) c.*413T>C (n.*413T>C) | |
| 12 | g.48966130A>T | CA384670911 | WNT10B | c.1135T>A (p.Cys379Ser) c.*417T>A (n.*417T>A) c.769T>A (p.Cys257Ser) c.*413T>A (n.*413T>A) | |
| 12 | g.48966131C>A | CA384670915 | WNT10B | c.1134G>T (p.Glu378Asp) c.*416G>T (n.*416G>T) c.768G>T (p.Glu256Asp) c.*412G>T (n.*412G>T) | |
| 12 | g.48966131C>G | CA384670918 | WNT10B | c.1134G>C (p.Glu378Asp) c.*416G>C (n.*416G>C) c.768G>C (p.Glu256Asp) c.*412G>C (n.*412G>C) | |
| 12 | g.48966131C>T | CA479703600 | WNT10B | c.1134G>A (p.Glu378=) c.*416G>A (n.*416G>A) c.768G>A (p.Glu256=) c.*412G>A (n.*412G>A) | |
| 12 | g.48966132T>A | CA384670925 | WNT10B | c.1133A>T (p.Glu378Val) c.*415A>T (n.*415A>T) c.767A>T (p.Glu256Val) c.*411A>T (n.*411A>T) | |
| 12 | g.48966132T>C | CA384670927 | WNT10B | c.1133A>G (p.Glu378Gly) c.*415A>G (n.*415A>G) c.767A>G (p.Glu256Gly) c.*411A>G (n.*411A>G) | |
| 12 | g.48966132T>G | CA384670922 | WNT10B | c.1133A>C (p.Glu378Ala) c.*415A>C (n.*415A>C) c.767A>C (p.Glu256Ala) c.*411A>C (n.*411A>C) | |
| 12 | g.48966133C>A | CA384670931 | WNT10B | c.1132G>T (p.Glu378Ter) c.*414G>T (n.*414G>T) c.766G>T (p.Glu256Ter) c.*410G>T (n.*410G>T) | |
| 12 | g.48966133C= | CA2034911787 | WNT10B | c.1132G= (p.Glu378=) c.*414G= (n.*414G=) c.766G= (p.Glu256=) c.*410G= (n.*410G=) | |
| 12 | g.48966133C>G | CA384670934 | WNT10B | c.1132G>C (p.Glu378Gln) c.*414G>C (n.*414G>C) c.766G>C (p.Glu256Gln) c.*410G>C (n.*410G>C) | |
| 12 | g.48966133C>T | CA384670937 | WNT10B | c.1132G>A (p.Glu378Lys) c.*414G>A (n.*414G>A) c.766G>A (p.Glu256Lys) c.*410G>A (n.*410G>A) | dbSNP gnomAD v2 gnomAD v4 |