Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.45850995C>GCA384480560ARID2c.2872C>G (p.Gln958Glu)
c.2793C>G
c.2425C>G (p.Gln809Glu)
c.1702C>G (p.Gln568Glu)
n.2163C>G
c.1240C>G (p.Gln414Glu)
n.3020C>G
n.3003C>G
dbSNP
12g.45850995C>ACA384480557ARID2c.2872C>A (p.Gln958Lys)
c.2793C>A
c.2425C>A (p.Gln809Lys)
c.1702C>A (p.Gln568Lys)
n.2163C>A
c.1240C>A (p.Gln414Lys)
n.3020C>A
n.3003C>A
dbSNP
12g.45850995C>TCA16607287ARID2c.2872C>T (p.Gln958Ter)
c.2793C>T
c.2425C>T (p.Gln809Ter)
c.1702C>T (p.Gln568Ter)
n.2163C>T
c.1240C>T (p.Gln414Ter)
n.3020C>T
n.3003C>T
ClinVar dbSNP COSMIC

Number of alleles fetched