Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157207091G>ACA150379161ARID1Bc.6160G>A (p.Glu2054Lys)
c.6229G>A (p.Glu2077Lys)
c.6448G>A (p.Glu2150Lys)
c.6199G>A (p.Glu2067Lys)
c.5911G>A (p.Glu1971Lys)
c.4477G>A (p.Glu1493Lys)
c.3640G>A (p.Glu1214Lys)
c.475G>A (p.Glu159Lys)
c.3271G>A (p.Glu1091Lys)
n.4782G>A
n.2239G>A
c.6319G>A (p.Glu2107Lys)
n.4316G>A
c.3687G>A
c.3601G>A
n.2985G>A
c.3661G>A (p.Glu1221Lys)
c.3820G>A (p.Glu1274Lys)
n.3434G>A
c.5950G>A (p.Glu1984Lys)
c.6070G>A (p.Glu2024Lys)
c.5149G>A (p.Glu1717Lys)
c.4969G>A (p.Glu1657Lys)
c.4729G>A (p.Glu1577Lys)
c.4348G>A (p.Glu1450Lys)
c.3211G>A (p.Glu1071Lys)
c.6280G>A (p.Glu2094Lys)
c.6181G>A (p.Glu2061Lys)
c.6151G>A (p.Glu2051Lys)
c.6121G>A (p.Glu2041Lys)
c.5992G>A (p.Glu1998Lys)
c.5971G>A (p.Glu1991Lys)
n.6266G>A
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.157207091G>TCA236275ARID1Bc.6160G>T (p.Glu2054Ter)
c.6229G>T (p.Glu2077Ter)
c.6448G>T (p.Glu2150Ter)
c.6199G>T (p.Glu2067Ter)
c.5911G>T (p.Glu1971Ter)
c.4477G>T (p.Glu1493Ter)
c.3640G>T (p.Glu1214Ter)
c.475G>T (p.Glu159Ter)
c.3271G>T (p.Glu1091Ter)
n.4782G>T
n.2239G>T
c.6319G>T (p.Glu2107Ter)
n.4316G>T
c.3687G>T
c.3601G>T
n.2985G>T
c.3661G>T (p.Glu1221Ter)
c.3820G>T (p.Glu1274Ter)
n.3434G>T
c.5950G>T (p.Glu1984Ter)
c.6070G>T (p.Glu2024Ter)
c.5149G>T (p.Glu1717Ter)
c.4969G>T (p.Glu1657Ter)
c.4729G>T (p.Glu1577Ter)
c.4348G>T (p.Glu1450Ter)
c.3211G>T (p.Glu1071Ter)
c.6280G>T (p.Glu2094Ter)
c.6181G>T (p.Glu2061Ter)
c.6151G>T (p.Glu2051Ter)
c.6121G>T (p.Glu2041Ter)
c.5992G>T (p.Glu1998Ter)
c.5971G>T (p.Glu1991Ter)
n.6266G>T
ClinVar dbSNP

Number of alleles fetched