Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.39023159G>ACA1624610SOS1n.1149C>T
c.36C>T (p.Asn12=)
n.1490C>T
n.1276C>T
c.1456C>T
c.1158C>T (p.Asn386=)
c.1269C>T (p.Asn423=)
n.113C>T
c.1362C>T (p.Asn454=)
c.1248C>T (p.Asn416=)
c.1245C>T (p.Asn415=)
c.1098C>T (p.Asn366=)
c.204C>T (p.Asn68=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.39023159G>CCA297301SOS1n.1149C>G
c.36C>G (p.Asn12Lys)
n.1490C>G
n.1276C>G
c.1456C>G
c.1158C>G (p.Asn386Lys)
c.1269C>G (p.Asn423Lys)
n.113C>G
c.1362C>G (p.Asn454Lys)
c.1248C>G (p.Asn416Lys)
c.1245C>G (p.Asn415Lys)
c.1098C>G (p.Asn366Lys)
c.204C>G (p.Asn68Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.39023159G>TCA346366560SOS1n.1149C>A
c.36C>A (p.Asn12Lys)
n.1490C>A
n.1276C>A
c.1456C>A
c.1158C>A (p.Asn386Lys)
c.1269C>A (p.Asn423Lys)
n.113C>A
c.1362C>A (p.Asn454Lys)
c.1248C>A (p.Asn416Lys)
c.1245C>A (p.Asn415Lys)
c.1098C>A (p.Asn366Lys)
c.204C>A (p.Asn68Lys)
ClinVar dbSNP gnomAD v4
2g.39023159G=CA1246140160SOS1n.1149C=
c.36C= (p.Asn12=)
n.1490C=
n.1276C=
c.1456C=
c.1158C= (p.Asn386=)
c.1269C= (p.Asn423=)
n.113C=
c.1362C= (p.Asn454=)
c.1248C= (p.Asn416=)
c.1245C= (p.Asn415=)
c.1098C= (p.Asn366=)
c.204C= (p.Asn68=)
dbSNP

Number of alleles fetched