Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.87268885_87268901delCA2573140128RASA1c.434_450del (p.Pro145ArgfsTer7)
dbSNP
5g.87268885_87268902delinsACA2739274823RASA1c.434_451delinsA (p.Pro145GlnfsTer7)
ClinVar
5g.87268895G>ACA445402376RASA1c.444G>A (p.Ala148=)
5g.87268895G>CCA445402377RASA1c.444G>C (p.Ala148=)
5g.87268895G=CA1561548144RASA1c.444G= (p.Ala148=)
5g.87268895G>TCA122462676RASA1c.444G>T (p.Ala148=)
dbSNP
5g.87268896G>ACA360417400RASA1c.445G>A (p.Gly149Ser)
5g.87268896G>CCA360417401RASA1c.445G>C (p.Gly149Arg)
5g.87268896G>TCA360417402RASA1c.445G>T (p.Gly149Cys)
5g.87268897G>ACA360417403RASA1c.446G>A (p.Gly149Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
5g.87268897G>CCA360417404RASA1c.446G>C (p.Gly149Ala)
5g.87268897G=CA1561548149RASA1c.446G= (p.Gly149=)
5g.87268897G>TCA360417405RASA1c.446G>T (p.Gly149Val)
5g.87268898C>ACA445402381RASA1c.447C>A (p.Gly149=)
5g.87268898C=CA1561548155RASA1c.447C= (p.Gly149=)
5g.87268898C>GCA445402380RASA1c.447C>G (p.Gly149=)
5g.87268898C>TCA3335436RASA1c.447C>T (p.Gly149=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.87268899C>ACA360417407RASA1c.448C>A (p.Leu150Ile)
5g.87268899C=CA1561548165RASA1c.448C= (p.Leu150=)
5g.87268899C>GCA360417406RASA1c.448C>G (p.Leu150Val)
5g.87268899C>TCA3335437RASA1c.448C>T (p.Leu150Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.87268900T>ACA360417408RASA1c.449T>A (p.Leu150His)
5g.87268900T>CCA360417409RASA1c.449T>C (p.Leu150Pro)
5g.87268900T>GCA360417410RASA1c.449T>G (p.Leu150Arg)
5g.87268901C>ACA445402385RASA1c.450C>A (p.Leu150=)
5g.87268901C>GCA445402386RASA1c.450C>G (p.Leu150=)
dbSNP
5g.87268901C>TCA445402387RASA1c.450C>T (p.Leu150=)
5g.87268902G>ACA360417411RASA1c.451G>A (p.Gly151Arg)
5g.87268902G>CCA360417412RASA1c.451G>C (p.Gly151Arg)
ClinVar gnomAD v4
5g.87268902G>TCA360417413RASA1c.451G>T (p.Gly151Trp)
5g.87268903G>ACA360417414RASA1c.452G>A (p.Gly151Glu)
5g.87268903G>CCA360417415RASA1c.452G>C (p.Gly151Ala)
5g.87268903G>TCA360417416RASA1c.452G>T (p.Gly151Val)
5g.87268904G>ACA3335438RASA1c.453G>A (p.Gly151=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.87268904G>CCA445402392RASA1c.453G>C (p.Gly151=)
ClinVar
5g.87268904G=CA1561548172RASA1c.453G= (p.Gly151=)
5g.87268904G>TCA445402391RASA1c.453G>T (p.Gly151=)
ClinVar dbSNP gnomAD v3 gnomAD v4
5g.87268905A=CA1561548181RASA1c.454A= (p.Thr152=)
5g.87268905A>CCA360417417RASA1c.454A>C (p.Thr152Pro)
5g.87268905A>GCA360417418RASA1c.454A>G (p.Thr152Ala)
ClinVar dbSNP gnomAD v4
5g.87268905A>TCA360417419RASA1c.454A>T (p.Thr152Ser)
5g.87268906C>ACA360417420RASA1c.455C>A (p.Thr152Lys)
5g.87268906C>GCA360417422RASA1c.455C>G (p.Thr152Arg)
5g.87268906C>TCA360417421RASA1c.455C>T (p.Thr152Ile)
gnomAD v4
5g.87268907A=CA1561548185RASA1c.456A= (p.Thr152=)
5g.87268907A>CCA445402393RASA1c.456A>C (p.Thr152=)
5g.87268907A>GCA3335439RASA1c.456A>G (p.Thr152=)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.87268907A>TCA445402397RASA1c.456A>T (p.Thr152=)
5g.87268908G>ACA360417423RASA1c.457G>A (p.Val153Met)
5g.87268908G>CCA360417424RASA1c.457G>C (p.Val153Leu)

Number of alleles fetched