Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.149379108A>C | CA365998154 | TAB2 | n.1608A>C c.1193A>C (p.Glu398Ala) c.341A>C (p.Glu114Ala) c.1097A>C (p.Glu366Ala) | |
6 | g.149379108A>G | CA365998155 | TAB2 | n.1608A>G c.1193A>G (p.Glu398Gly) c.341A>G (p.Glu114Gly) c.1097A>G (p.Glu366Gly) | |
6 | g.149379108A>T | CA365998156 | TAB2 | n.1608A>T c.1193A>T (p.Glu398Val) c.341A>T (p.Glu114Val) c.1097A>T (p.Glu366Val) | |
6 | g.149379109A>C | CA365998158 | TAB2 | n.1609A>C c.1194A>C (p.Glu398Asp) c.342A>C (p.Glu114Asp) c.1098A>C (p.Glu366Asp) | |
6 | g.149379109A>G | CA452720637 | TAB2 | n.1609A>G c.1194A>G (p.Glu398=) c.342A>G (p.Glu114=) c.1098A>G (p.Glu366=) | gnomAD v4 |
6 | g.149379109A>T | CA365998157 | TAB2 | n.1609A>T c.1194A>T (p.Glu398Asp) c.342A>T (p.Glu114Asp) c.1098A>T (p.Glu366Asp) | |
6 | g.149379110C>A | CA365998159 | TAB2 | n.1610C>A c.1195C>A (p.Gln399Lys) c.343C>A (p.Gln115Lys) c.1099C>A (p.Gln367Lys) | |
6 | g.149379110C= | CA1671916027 | TAB2 | n.1610C= c.1195C= (p.Gln399=) c.343C= (p.Gln115=) c.1099C= (p.Gln367=) | |
6 | g.149379110C>G | CA365998160 | TAB2 | n.1610C>G c.1195C>G (p.Gln399Glu) c.343C>G (p.Gln115Glu) c.1099C>G (p.Gln367Glu) | |
6 | g.149379110C>T | CA16042638 | TAB2 | n.1610C>T c.1195C>T (p.Gln399Ter) c.343C>T (p.Gln115Ter) c.1099C>T (p.Gln367Ter) | ClinVar dbSNP |
6 | g.149379111A>C | CA365998161 | TAB2 | n.1611A>C c.1196A>C (p.Gln399Pro) c.344A>C (p.Gln115Pro) c.1100A>C (p.Gln367Pro) | |
6 | g.149379111A>G | CA365998162 | TAB2 | n.1611A>G c.1196A>G (p.Gln399Arg) c.344A>G (p.Gln115Arg) c.1100A>G (p.Gln367Arg) | |
6 | g.149379111A>T | CA365998163 | TAB2 | n.1611A>T c.1196A>T (p.Gln399Leu) c.344A>T (p.Gln115Leu) c.1100A>T (p.Gln367Leu) | |
6 | g.149379112G>A | CA4041508 | TAB2 | n.1612G>A c.1197G>A (p.Gln399=) c.345G>A (p.Gln115=) c.1101G>A (p.Gln367=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.149379112G>C | CA365998165 | TAB2 | n.1612G>C c.1197G>C (p.Gln399His) c.345G>C (p.Gln115His) c.1101G>C (p.Gln367His) | |
6 | g.149379112G= | CA1671916030 | TAB2 | n.1612G= c.1197G= (p.Gln399=) c.345G= (p.Gln115=) c.1101G= (p.Gln367=) | |
6 | g.149379112G>T | CA365998164 | TAB2 | n.1612G>T c.1197G>T (p.Gln399His) c.345G>T (p.Gln115His) c.1101G>T (p.Gln367His) | |
6 | g.149379113G>A | CA365998166 | TAB2 | n.1613G>A c.1198G>A (p.Val400Ile) c.346G>A (p.Val116Ile) c.1102G>A (p.Val368Ile) | gnomAD v4 |
6 | g.149379113G>C | CA365998167 | TAB2 | n.1613G>C c.1198G>C (p.Val400Leu) c.346G>C (p.Val116Leu) c.1102G>C (p.Val368Leu) | |
6 | g.149379113G>T | CA365998168 | TAB2 | n.1613G>T c.1198G>T (p.Val400Phe) c.346G>T (p.Val116Phe) c.1102G>T (p.Val368Phe) | |
6 | g.149379114T>A | CA365998169 | TAB2 | n.1614T>A c.1199T>A (p.Val400Asp) c.347T>A (p.Val116Asp) c.1103T>A (p.Val368Asp) | dbSNP |
6 | g.149379114T>C | CA365998170 | TAB2 | n.1614T>C c.1199T>C (p.Val400Ala) c.347T>C (p.Val116Ala) c.1103T>C (p.Val368Ala) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.149379114T>G | CA365998171 | TAB2 | n.1614T>G c.1199T>G (p.Val400Gly) c.347T>G (p.Val116Gly) c.1103T>G (p.Val368Gly) | |
6 | g.149379114T= | CA1671916035 | TAB2 | n.1614T= c.1199T= (p.Val400=) c.347T= (p.Val116=) c.1103T= (p.Val368=) | |
6 | g.149379115C>A | CA452720664 | TAB2 | n.1615C>A c.1200C>A (p.Val400=) c.348C>A (p.Val116=) c.1104C>A (p.Val368=) | |
6 | g.149379115C= | CA1671916039 | TAB2 | n.1615C= c.1200C= (p.Val400=) c.348C= (p.Val116=) c.1104C= (p.Val368=) | |
6 | g.149379115C>G | CA452720661 | TAB2 | n.1615C>G c.1200C>G (p.Val400=) c.348C>G (p.Val116=) c.1104C>G (p.Val368=) | dbSNP |
6 | g.149379115C>T | CA452720660 | TAB2 | n.1615C>T c.1200C>T (p.Val400=) c.348C>T (p.Val116=) c.1104C>T (p.Val368=) | |
6 | g.149379116A= | CA1671916043 | TAB2 | n.1616A= c.1201A= (p.Met401=) c.349A= (p.Met117=) c.1105A= (p.Met369=) | |
6 | g.149379116A>C | CA365998172 | TAB2 | n.1616A>C c.1201A>C (p.Met401Leu) c.349A>C (p.Met117Leu) c.1105A>C (p.Met369Leu) | |
6 | g.149379116A>G | CA365998174 | TAB2 | n.1616A>G c.1201A>G (p.Met401Val) c.349A>G (p.Met117Val) c.1105A>G (p.Met369Val) | dbSNP gnomAD v4 |
6 | g.149379116A>T | CA365998173 | TAB2 | n.1616A>T c.1201A>T (p.Met401Leu) c.349A>T (p.Met117Leu) c.1105A>T (p.Met369Leu) | |
6 | g.149379117T>A | CA365998175 | TAB2 | n.1617T>A c.1202T>A (p.Met401Lys) c.350T>A (p.Met117Lys) c.1106T>A (p.Met369Lys) | |
6 | g.149379117T>C | CA365998176 | TAB2 | n.1617T>C c.1202T>C (p.Met401Thr) c.350T>C (p.Met117Thr) c.1106T>C (p.Met369Thr) | dbSNP |
6 | g.149379117T>G | CA365998177 | TAB2 | n.1617T>G c.1202T>G (p.Met401Arg) c.350T>G (p.Met117Arg) c.1106T>G (p.Met369Arg) | |
6 | g.149379117T= | CA1671916046 | TAB2 | n.1617T= c.1202T= (p.Met401=) c.350T= (p.Met117=) c.1106T= (p.Met369=) | |
6 | g.149379118G>A | CA365998178 | TAB2 | n.1618G>A c.1203G>A (p.Met401Ile) c.351G>A (p.Met117Ile) c.1107G>A (p.Met369Ile) | gnomAD v4 |
6 | g.149379118G>C | CA365998179 | TAB2 | n.1618G>C c.1203G>C (p.Met401Ile) c.351G>C (p.Met117Ile) c.1107G>C (p.Met369Ile) | |
6 | g.149379118G>T | CA365998180 | TAB2 | n.1618G>T c.1203G>T (p.Met401Ile) c.351G>T (p.Met117Ile) c.1107G>T (p.Met369Ile) | |
6 | g.149379119C>A | CA452720675 | TAB2 | n.1619C>A c.1204C>A (p.Arg402=) c.352C>A (p.Arg118=) c.1108C>A (p.Arg370=) | |
6 | g.149379119C= | CA1671916048 | TAB2 | n.1619C= c.1204C= (p.Arg402=) c.352C= (p.Arg118=) c.1108C= (p.Arg370=) | |
6 | g.149379119C>G | CA365998181 | TAB2 | n.1619C>G c.1204C>G (p.Arg402Gly) c.352C>G (p.Arg118Gly) c.1108C>G (p.Arg370Gly) | |
6 | g.149379119C>T | CA4041509 | TAB2 | n.1619C>T c.1204C>T (p.Arg402Trp) c.352C>T (p.Arg118Trp) c.1108C>T (p.Arg370Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.149379120G>A | CA365998182 | TAB2 | n.1620G>A c.1205G>A (p.Arg402Gln) c.353G>A (p.Arg118Gln) c.1109G>A (p.Arg370Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
6 | g.149379120G>C | CA365998183 | TAB2 | n.1620G>C c.1205G>C (p.Arg402Pro) c.353G>C (p.Arg118Pro) c.1109G>C (p.Arg370Pro) | |
6 | g.149379120G= | CA1671916052 | TAB2 | n.1620G= c.1205G= (p.Arg402=) c.353G= (p.Arg118=) c.1109G= (p.Arg370=) | |
6 | g.149379120G>T | CA365998184 | TAB2 | n.1620G>T c.1205G>T (p.Arg402Leu) c.353G>T (p.Arg118Leu) c.1109G>T (p.Arg370Leu) | |
6 | g.149379121G>A | CA452720682 | TAB2 | n.1621G>A c.1206G>A (p.Arg402=) c.354G>A (p.Arg118=) c.1110G>A (p.Arg370=) | |
6 | g.149379121G>C | CA452720689 | TAB2 | n.1621G>C c.1206G>C (p.Arg402=) c.354G>C (p.Arg118=) c.1110G>C (p.Arg370=) | COSMIC |
6 | g.149379121G>T | CA452720692 | TAB2 | n.1621G>T c.1206G>T (p.Arg402=) c.354G>T (p.Arg118=) c.1110G>T (p.Arg370=) |