Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154863115A=CA2466815612F8c.6542T= (p.Leu2181=)
c.275T= (p.Leu92=)
c.137T= (p.Leu46=)
c.6437T= (p.Leu2146=)
Xg.154863115A>CCA414907097F8c.6542T>G (p.Leu2181Arg)
c.275T>G (p.Leu92Arg)
c.137T>G (p.Leu46Arg)
c.6437T>G (p.Leu2146Arg)
Xg.154863115A>GCA414907098F8c.6542T>C (p.Leu2181Pro)
c.275T>C (p.Leu92Pro)
c.137T>C (p.Leu46Pro)
c.6437T>C (p.Leu2146Pro)
dbSNP
Xg.154863115A>TCA414907101F8c.6542T>A (p.Leu2181His)
c.275T>A (p.Leu92His)
c.137T>A (p.Leu46His)
c.6437T>A (p.Leu2146His)
Xg.154863116G>ACA414907104F8c.6541C>T (p.Leu2181Phe)
c.274C>T (p.Leu92Phe)
c.136C>T (p.Leu46Phe)
c.6436C>T (p.Leu2146Phe)
dbSNP
Xg.154863116G>CCA414907105F8c.6541C>G (p.Leu2181Val)
c.274C>G (p.Leu92Val)
c.136C>G (p.Leu46Val)
c.6436C>G (p.Leu2146Val)
Xg.154863116G=CA2466815615F8c.6541C= (p.Leu2181=)
c.274C= (p.Leu92=)
c.136C= (p.Leu46=)
c.6436C= (p.Leu2146=)
Xg.154863116G>TCA414907106F8c.6541C>A (p.Leu2181Ile)
c.274C>A (p.Leu92Ile)
c.136C>A (p.Leu46Ile)
c.6436C>A (p.Leu2146Ile)
Xg.154863117A>CCA519357840F8c.6540T>G (p.Thr2180=)
c.273T>G (p.Thr91=)
c.135T>G (p.Thr45=)
c.6435T>G (p.Thr2145=)
Xg.154863117A>GCA519357841F8c.6540T>C (p.Thr2180=)
c.273T>C (p.Thr91=)
c.135T>C (p.Thr45=)
c.6435T>C (p.Thr2145=)
Xg.154863117A>TCA519357843F8c.6540T>A (p.Thr2180=)
c.273T>A (p.Thr91=)
c.135T>A (p.Thr45=)
c.6435T>A (p.Thr2145=)
Xg.154863118G>ACA414907109F8c.6539C>T (p.Thr2180Ile)
c.272C>T (p.Thr91Ile)
c.134C>T (p.Thr45Ile)
c.6434C>T (p.Thr2145Ile)
dbSNP
Xg.154863118G>CCA414907122F8c.6539C>G (p.Thr2180Ser)
c.272C>G (p.Thr91Ser)
c.134C>G (p.Thr45Ser)
c.6434C>G (p.Thr2145Ser)
Xg.154863118G=CA2466815617F8c.6539C= (p.Thr2180=)
c.272C= (p.Thr91=)
c.134C= (p.Thr45=)
c.6434C= (p.Thr2145=)
Xg.154863118G>TCA414907111F8c.6539C>A (p.Thr2180Asn)
c.272C>A (p.Thr91Asn)
c.134C>A (p.Thr45Asn)
c.6434C>A (p.Thr2145Asn)
Xg.154863119T>ACA414907126F8c.6538A>T (p.Thr2180Ser)
c.271A>T (p.Thr91Ser)
c.133A>T (p.Thr45Ser)
c.6433A>T (p.Thr2145Ser)
Xg.154863119T>CCA414907146F8c.6538A>G (p.Thr2180Ala)
c.271A>G (p.Thr91Ala)
c.133A>G (p.Thr45Ala)
c.6433A>G (p.Thr2145Ala)
Xg.154863119T>GCA414907147F8c.6538A>C (p.Thr2180Pro)
c.271A>C (p.Thr91Pro)
c.133A>C (p.Thr45Pro)
c.6433A>C (p.Thr2145Pro)
Xg.154863120G>ACA519357848F8c.6537C>T (p.Ser2179=)
c.270C>T (p.Ser90=)
c.132C>T (p.Ser44=)
c.6432C>T (p.Ser2144=)
Xg.154863120G>CCA414907148F8c.6537C>G (p.Ser2179Arg)
c.270C>G (p.Ser90Arg)
c.132C>G (p.Ser44Arg)
c.6432C>G (p.Ser2144Arg)
Xg.154863120G>TCA414907150F8c.6537C>A (p.Ser2179Arg)
c.270C>A (p.Ser90Arg)
c.132C>A (p.Ser44Arg)
c.6432C>A (p.Ser2144Arg)
Xg.154863121delCA2695237166F8c.6536del (p.Ser2179ThrfsTer7)
c.269del (p.Ser90ThrfsTer7)
c.131del (p.Ser44ThrfsTer7)
c.6431del (p.Ser2144ThrfsTer7)
Xg.154863121C>ACA414907163F8c.6536G>T (p.Ser2179Ile)
c.269G>T (p.Ser90Ile)
c.131G>T (p.Ser44Ile)
c.6431G>T (p.Ser2144Ile)
Xg.154863121C=CA2466815620F8c.6536G= (p.Ser2179=)
c.269G= (p.Ser90=)
c.131G= (p.Ser44=)
c.6431G= (p.Ser2144=)
Xg.154863121C>GCA414907166F8c.6536G>C (p.Ser2179Thr)
c.269G>C (p.Ser90Thr)
c.131G>C (p.Ser44Thr)
c.6431G>C (p.Ser2144Thr)
Xg.154863121C>TCA414907171F8c.6536G>A (p.Ser2179Asn)
c.269G>A (p.Ser90Asn)
c.131G>A (p.Ser44Asn)
c.6431G>A (p.Ser2144Asn)
dbSNP gnomAD v3 gnomAD v4
Xg.154863122T>ACA414907175F8c.6535A>T (p.Ser2179Cys)
c.268A>T (p.Ser90Cys)
c.130A>T (p.Ser44Cys)
c.6430A>T (p.Ser2144Cys)
Xg.154863122T>CCA414907176F8c.6535A>G (p.Ser2179Gly)
c.268A>G (p.Ser90Gly)
c.130A>G (p.Ser44Gly)
c.6430A>G (p.Ser2144Gly)
Xg.154863122T>GCA414907178F8c.6535A>C (p.Ser2179Arg)
c.268A>C (p.Ser90Arg)
c.130A>C (p.Ser44Arg)
c.6430A>C (p.Ser2144Arg)
Xg.154863123G>ACA519357854F8c.6534C>T (p.Arg2178=)
c.267C>T (p.Arg89=)
c.129C>T (p.Arg43=)
c.6429C>T (p.Arg2143=)
Xg.154863123G>CCA519357856F8c.6534C>G (p.Arg2178=)
c.267C>G (p.Arg89=)
c.129C>G (p.Arg43=)
c.6429C>G (p.Arg2143=)
Xg.154863123G>TCA519357858F8c.6534C>A (p.Arg2178=)
c.267C>A (p.Arg89=)
c.129C>A (p.Arg43=)
c.6429C>A (p.Arg2143=)
Xg.154863124C>ACA255207F8c.6533G>T (p.Arg2178Leu)
c.266G>T (p.Arg89Leu)
c.128G>T (p.Arg43Leu)
c.6428G>T (p.Arg2143Leu)
ClinVar dbSNP
Xg.154863124C=CA2466815624F8c.6533G= (p.Arg2178=)
c.266G= (p.Arg89=)
c.128G= (p.Arg43=)
c.6428G= (p.Arg2143=)
Xg.154863124C>GCA414907187F8c.6533G>C (p.Arg2178Pro)
c.266G>C (p.Arg89Pro)
c.128G>C (p.Arg43Pro)
c.6428G>C (p.Arg2143Pro)
Xg.154863124C>TCA255212F8c.6533G>A (p.Arg2178His)
c.266G>A (p.Arg89His)
c.128G>A (p.Arg43His)
c.6428G>A (p.Arg2143His)
ClinVar dbSNP ExAC gnomAD v4 COSMIC COSMIC
Xg.154863125G>ACA255211F8c.6532C>T (p.Arg2178Cys)
c.265C>T (p.Arg89Cys)
c.127C>T (p.Arg43Cys)
c.6427C>T (p.Arg2143Cys)
ClinVar dbSNP ExAC gnomAD v4 COSMIC COSMIC
Xg.154863125G>CCA414907205F8c.6532C>G (p.Arg2178Gly)
c.265C>G (p.Arg89Gly)
c.127C>G (p.Arg43Gly)
c.6427C>G (p.Arg2143Gly)
Xg.154863125G=CA2466815631F8c.6532C= (p.Arg2178=)
c.265C= (p.Arg89=)
c.127C= (p.Arg43=)
c.6427C= (p.Arg2143=)
Xg.154863125G>TCA414907212F8c.6532C>A (p.Arg2178Ser)
c.265C>A (p.Arg89Ser)
c.127C>A (p.Arg43Ser)
c.6427C>A (p.Arg2143Ser)
Xg.154863126A>CCA414907217F8c.6531T>G (p.Ile2177Met)
c.264T>G (p.Ile88Met)
c.126T>G (p.Ile42Met)
c.6426T>G (p.Ile2142Met)
Xg.154863126A>GCA519357862F8c.6531T>C (p.Ile2177=)
c.264T>C (p.Ile88=)
c.126T>C (p.Ile42=)
c.6426T>C (p.Ile2142=)
Xg.154863126A>TCA519357863F8c.6531T>A (p.Ile2177=)
c.264T>A (p.Ile88=)
c.126T>A (p.Ile42=)
c.6426T>A (p.Ile2142=)
Xg.154863127A>CCA414907225F8c.6530T>G (p.Ile2177Ser)
c.263T>G (p.Ile88Ser)
c.125T>G (p.Ile42Ser)
c.6425T>G (p.Ile2142Ser)
Xg.154863127A>GCA414907223F8c.6530T>C (p.Ile2177Thr)
c.263T>C (p.Ile88Thr)
c.125T>C (p.Ile42Thr)
c.6425T>C (p.Ile2142Thr)
Xg.154863127A>TCA414907228F8c.6530T>A (p.Ile2177Asn)
c.263T>A (p.Ile88Asn)
c.125T>A (p.Ile42Asn)
c.6425T>A (p.Ile2142Asn)
Xg.154863128T>ACA414907232F8c.6529A>T (p.Ile2177Phe)
c.262A>T (p.Ile88Phe)
c.124A>T (p.Ile42Phe)
c.6424A>T (p.Ile2142Phe)
Xg.154863128T>CCA414907234F8c.6529A>G (p.Ile2177Val)
c.262A>G (p.Ile88Val)
c.124A>G (p.Ile42Val)
c.6424A>G (p.Ile2142Val)
Xg.154863128T>GCA414907236F8c.6529A>C (p.Ile2177Leu)
c.262A>C (p.Ile88Leu)
c.124A>C (p.Ile42Leu)
c.6424A>C (p.Ile2142Leu)
Xg.154863129G>ACA519357867F8c.6528C>T (p.Ser2176=)
c.261C>T (p.Ser87=)
c.123C>T (p.Ser41=)
c.6423C>T (p.Ser2141=)
COSMIC COSMIC

Number of alleles fetched