Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.26773394G>CCA339168559ARID1Ac.3764G>C (p.Gly1255Ala)
c.2615G>C (p.Gly872Ala)
c.2612G>C (p.Gly871Ala)
c.73G>C
n.74G>C
c.2618G>C (p.Gly873Ala)
n.70G>C
c.453G>C
dbSNP
1g.26773394G>TCA339168560ARID1Ac.3764G>T (p.Gly1255Val)
c.2615G>T (p.Gly872Val)
c.2612G>T (p.Gly871Val)
c.73G>T
n.74G>T
c.2618G>T (p.Gly873Val)
n.70G>T
c.453G>T
dbSNP
1g.26773394G>ACA339168557ARID1Ac.3764G>A (p.Gly1255Glu)
c.2615G>A (p.Gly872Glu)
c.2612G>A (p.Gly871Glu)
c.73G>A
n.74G>A
c.2618G>A (p.Gly873Glu)
n.70G>A
c.453G>A
ClinVar dbSNP

Number of alleles fetched