Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.8059732C>ACA383798903C3AR1c.454G>T (p.Val152Leu)
12g.8059732C>GCA383798904C3AR1c.454G>C (p.Val152Leu)
12g.8059732C>TCA383798905C3AR1c.454G>A (p.Val152Met)
12g.8059732_8059733delinsCACA2014849546C3AR1c.453_454delinsTG (p.Phe151=)
12g.8059733A>CCA383798906C3AR1c.453T>G (p.Phe151Leu)
12g.8059733A>GCA478528884C3AR1c.453T>C (p.Phe151=)
12g.8059733A>TCA383798907C3AR1c.453T>A (p.Phe151Leu)
12g.8059736delCA232559536C3AR1c.453del (p.Phe151LeufsTer2)
dbSNP gnomAD v3 gnomAD v4
12g.8059734A>CCA383798908C3AR1c.452T>G (p.Phe151Cys)
12g.8059734A>GCA383798909C3AR1c.452T>C (p.Phe151Ser)
12g.8059734A>TCA383798910C3AR1c.452T>A (p.Phe151Tyr)
12g.8059735A=CA2014849547C3AR1c.451T= (p.Phe151=)
12g.8059735A>CCA383798912C3AR1c.451T>G (p.Phe151Val)
12g.8059735A>GCA6432008C3AR1c.451T>C (p.Phe151Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.8059735A>TCA383798911C3AR1c.451T>A (p.Phe151Ile)
12g.8059736A>CCA478528891C3AR1c.450T>G (p.Ala150=)
12g.8059736A>GCA478528894C3AR1c.450T>C (p.Ala150=)
12g.8059736A>TCA478528893C3AR1c.450T>A (p.Ala150=)
12g.8059737G>ACA383798914C3AR1c.449C>T (p.Ala150Val)
gnomAD v4
12g.8059737G>CCA383798916C3AR1c.449C>G (p.Ala150Gly)
dbSNP gnomAD v2 gnomAD v4
12g.8059737G=CA2014849548C3AR1c.449C= (p.Ala150=)
12g.8059737G>TCA383798918C3AR1c.449C>A (p.Ala150Asp)
ClinVar dbSNP
12g.8059738C>ACA383798919C3AR1c.448G>T (p.Ala150Ser)
12g.8059738C=CA2014849549C3AR1c.448G= (p.Ala150=)
12g.8059738C>GCA232559557C3AR1c.448G>C (p.Ala150Pro)
dbSNP gnomAD v3 gnomAD v4
12g.8059738C>TCA383798922C3AR1c.448G>A (p.Ala150Thr)
12g.8059739C>ACA478528896C3AR1c.447G>T (p.Val149=)
12g.8059739C=CA2014849550C3AR1c.447G= (p.Val149=)
12g.8059739C>GCA478528897C3AR1c.447G>C (p.Val149=)
12g.8059739C>TCA478528898C3AR1c.447G>A (p.Val149=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.8059740A>CCA383798924C3AR1c.446T>G (p.Val149Gly)
12g.8059740A>GCA383798926C3AR1c.446T>C (p.Val149Ala)
12g.8059740A>TCA383798928C3AR1c.446T>A (p.Val149Glu)
12g.8059741C>ACA383798930C3AR1c.445G>T (p.Val149Leu)
COSMIC
12g.8059741C>GCA383798932C3AR1c.445G>C (p.Val149Leu)
12g.8059741C>TCA383798933C3AR1c.445G>A (p.Val149Met)
gnomAD v4
12g.8059742C>ACA478528900C3AR1c.444G>T (p.Val148=)
dbSNP
12g.8059742C=CA2014849551C3AR1c.444G= (p.Val148=)
12g.8059742C>GCA478528901C3AR1c.444G>C (p.Val148=)
12g.8059742C>TCA478528903C3AR1c.444G>A (p.Val148=)
12g.8059743A=CA2014849552C3AR1c.443T= (p.Val148=)
12g.8059743A>CCA383798935C3AR1c.443T>G (p.Val148Gly)
dbSNP gnomAD v2 gnomAD v4
12g.8059743A>GCA383798937C3AR1c.443T>C (p.Val148Ala)
dbSNP gnomAD v4
12g.8059743A>TCA383798934C3AR1c.443T>A (p.Val148Glu)
12g.8059744C>ACA383798940C3AR1c.442G>T (p.Val148Leu)
12g.8059744C=CA2014849553C3AR1c.442G= (p.Val148=)
12g.8059744C>GCA383798941C3AR1c.442G>C (p.Val148Leu)
12g.8059744C>TCA383798943C3AR1c.442G>A (p.Val148Met)
dbSNP gnomAD v4
12g.8059745C>ACA383798945C3AR1c.441G>T (p.Trp147Cys)
12g.8059745C>GCA383798947C3AR1c.441G>C (p.Trp147Cys)

Number of alleles fetched