Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.20189132_20189151del | CA2695217664 | GJB2 | c.431_450del (p.Val144AspfsTer?) | |
13 | g.20189133_20189151del | CA2695217665 | GJB2 | c.431_449del (p.Val144AlafsTer18) | |
13 | g.20189146_20189149delinsAGAT | CA2077139221 | GJB2 | c.433_436delinsATCT (p.Ile145=) | |
13 | g.20189149_20189151del | CA246460156 | GJB2 | c.433_435del (p.Ile145del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.20189149T>A | CA387461158 | GJB2 | c.433A>T (p.Ile145Phe) | |
13 | g.20189149T>C | CA387461159 | GJB2 | c.433A>G (p.Ile145Val) | |
13 | g.20189149T>G | CA387461160 | GJB2 | c.433A>C (p.Ile145Leu) | |
13 | g.20189150G>A | CA483153960 | GJB2 | c.432C>T (p.Val144=) | ClinVar |
13 | g.20189150G>C | CA483153961 | GJB2 | c.432C>G (p.Val144=) | |
13 | g.20189150G>T | CA483153962 | GJB2 | c.432C>A (p.Val144=) | ClinVar gnomAD v4 |
13 | g.20189151A>C | CA387461163 | GJB2 | c.431T>G (p.Val144Gly) | |
13 | g.20189151A>G | CA387461162 | GJB2 | c.431T>C (p.Val144Ala) | |
13 | g.20189151A>T | CA387461161 | GJB2 | c.431T>A (p.Val144Asp) | |
13 | g.20189152C>A | CA387461164 | GJB2 | c.430G>T (p.Val144Phe) | |
13 | g.20189152C= | CA2077139234 | GJB2 | c.430G= (p.Val144=) | |
13 | g.20189152C>G | CA387461165 | GJB2 | c.430G>C (p.Val144Leu) | gnomAD v4 |
13 | g.20189152C>T | CA387461166 | GJB2 | c.430G>A (p.Val144Ile) | dbSNP |
13 | g.20189153C>A | CA483153963 | GJB2 | c.429G>T (p.Arg143=) | ClinVar dbSNP gnomAD v4 |
13 | g.20189153C>G | CA483153964 | GJB2 | c.429G>C (p.Arg143=) | |
13 | g.20189153C>T | CA483153965 | GJB2 | c.429G>A (p.Arg143=) | gnomAD v4 |
13 | g.20189154C>A | CA387461167 | GJB2 | c.428G>T (p.Arg143Leu) | gnomAD v4 |
13 | g.20189154C= | CA2077139238 | GJB2 | c.428G= (p.Arg143=) | |
13 | g.20189154C>G | CA387461168 | GJB2 | c.428G>C (p.Arg143Pro) | |
13 | g.20189154C>T | CA257677 | GJB2 | c.428G>A (p.Arg143Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
13 | g.20189155G>A | CA172234 | GJB2 | c.427C>T (p.Arg143Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.20189155G>C | CA387461169 | GJB2 | c.427C>G (p.Arg143Gly) | |
13 | g.20189155G= | CA2077139242 | GJB2 | c.427C= (p.Arg143=) | |
13 | g.20189155G>T | CA483153966 | GJB2 | c.427C>A (p.Arg143=) | |
13 | g.20189156G>A | CA483153967 | GJB2 | c.426C>T (p.Phe142=) | gnomAD v4 |
13 | g.20189156G>C | CA387461170 | GJB2 | c.426C>G (p.Phe142Leu) | |
13 | g.20189156G= | CA2077139248 | GJB2 | c.426C= (p.Phe142=) | |
13 | g.20189156G>T | CA261647 | GJB2 | c.426C>A (p.Phe142Leu) | ClinVar dbSNP |
13 | g.20189161_20189163del | CA2580614612 | GJB2 | c.424_426del (p.Phe142del) | ClinVar |
13 | g.20189157A= | CA2077139253 | GJB2 | c.425T= (p.Phe142=) | |
13 | g.20189157A>C | CA387461171 | GJB2 | c.425T>G (p.Phe142Cys) | gnomAD v4 |
13 | g.20189157A>G | CA6904271 | GJB2 | c.425T>C (p.Phe142Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.20189157A>T | CA387461172 | GJB2 | c.425T>A (p.Phe142Tyr) | |
13 | g.20189158A>C | CA387461174 | GJB2 | c.424T>G (p.Phe142Val) | |
13 | g.20189158A>G | CA387461175 | GJB2 | c.424T>C (p.Phe142Leu) | |
13 | g.20189158A>T | CA387461173 | GJB2 | c.424T>A (p.Phe142Ile) | |
13 | g.20189159G>A | CA483153968 | GJB2 | c.423C>T (p.Phe141=) | ClinVar gnomAD v4 |
13 | g.20189159G>C | CA387461176 | GJB2 | c.423C>G (p.Phe141Leu) | COSMIC |
13 | g.20189159G>T | CA387461177 | GJB2 | c.423C>A (p.Phe141Leu) | |
13 | g.20189160A>C | CA387461178 | GJB2 | c.422T>G (p.Phe141Cys) | |
13 | g.20189160A>G | CA387461179 | GJB2 | c.422T>C (p.Phe141Ser) | |
13 | g.20189160A>T | CA387461180 | GJB2 | c.422T>A (p.Phe141Tyr) | |
13 | g.20189161A>C | CA387461181 | GJB2 | c.421T>G (p.Phe141Val) | |
13 | g.20189161A>G | CA387461182 | GJB2 | c.421T>C (p.Phe141Leu) | |
13 | g.20189161A>T | CA387461183 | GJB2 | c.421T>A (p.Phe141Ile) | |
13 | g.20189162G>A | CA483153969 | GJB2 | c.420C>T (p.Ile140=) | ClinVar dbSNP gnomAD v4 COSMIC |