Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.37739602A>C | CA398751663 | HNF1B | c.382T>G (p.Tyr128Asp) | |
17 | g.37739602A>G | CA398751664 | HNF1B | c.382T>C (p.Tyr128His) | |
17 | g.37739602A>T | CA398751665 | HNF1B | c.382T>A (p.Tyr128Asn) | |
17 | g.37739603dup | CA983445274 | HNF1B | c.382dup (p.Tyr128LeufsTer?) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739603A>C | CA499603973 | HNF1B | c.381T>G (p.Gly127=) | |
17 | g.37739603A>G | CA8519078 | HNF1B | c.381T>C (p.Gly127=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739603A>T | CA499603972 | HNF1B | c.381T>A (p.Gly127=) | |
17 | g.37739604C>A | CA398751667 | HNF1B | c.380G>T (p.Gly127Val) | |
17 | g.37739604C>G | CA398751668 | HNF1B | c.380G>C (p.Gly127Ala) | |
17 | g.37739604C>T | CA398751670 | HNF1B | c.380G>A (p.Gly127Asp) | |
17 | g.37739605C>A | CA398751673 | HNF1B | c.379G>T (p.Gly127Cys) | gnomAD v4 |
17 | g.37739605C>G | CA398751675 | HNF1B | c.379G>C (p.Gly127Arg) | gnomAD v4 |
17 | g.37739605C>T | CA398751672 | HNF1B | c.379G>A (p.Gly127Ser) | |
17 | g.37739606C>A | CA398751679 | HNF1B | c.378G>T (p.Lys126Asn) | |
17 | g.37739606C>G | CA398751677 | HNF1B | c.378G>C (p.Lys126Asn) | |
17 | g.37739606C>T | CA499603974 | HNF1B | c.378G>A (p.Lys126=) | |
17 | g.37739607T>A | CA398751684 | HNF1B | c.377A>T (p.Lys126Met) | |
17 | g.37739607T>C | CA398751680 | HNF1B | c.377A>G (p.Lys126Arg) | gnomAD v4 |
17 | g.37739607T>G | CA398751682 | HNF1B | c.377A>C (p.Lys126Thr) | |
17 | g.37739608T>A | CA398751686 | HNF1B | c.376A>T (p.Lys126Ter) | |
17 | g.37739608T>C | CA398751687 | HNF1B | c.376A>G (p.Lys126Glu) | ClinVar |
17 | g.37739608T>G | CA398751688 | HNF1B | c.376A>C (p.Lys126Gln) | |
17 | g.37739609G>A | CA499603975 | HNF1B | c.375C>T (p.Ile125=) | |
17 | g.37739609G>C | CA398751689 | HNF1B | c.375C>G (p.Ile125Met) | dbSNP |
17 | g.37739609G>T | CA8519079 | HNF1B | c.375C>A (p.Ile125=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739610A>C | CA398751690 | HNF1B | c.374T>G (p.Ile125Ser) | |
17 | g.37739610A>G | CA398751691 | HNF1B | c.374T>C (p.Ile125Thr) | ClinVar |
17 | g.37739610A>T | CA398751692 | HNF1B | c.374T>A (p.Ile125Asn) | ClinVar dbSNP |
17 | g.37739611T>A | CA398751693 | HNF1B | c.373A>T (p.Ile125Phe) | |
17 | g.37739611T>C | CA398751694 | HNF1B | c.373A>G (p.Ile125Val) | |
17 | g.37739611T>G | CA398751695 | HNF1B | c.373A>C (p.Ile125Leu) | |
17 | g.37739612C>A | CA398751698 | HNF1B | c.372G>T (p.Met124Ile) | ClinVar |
17 | g.37739612C>G | CA398751697 | HNF1B | c.372G>C (p.Met124Ile) | |
17 | g.37739612C>T | CA398751696 | HNF1B | c.372G>A (p.Met124Ile) | |
17 | g.37739613A>C | CA398751699 | HNF1B | c.371T>G (p.Met124Arg) | |
17 | g.37739613A>G | CA398751700 | HNF1B | c.371T>C (p.Met124Thr) | |
17 | g.37739613A>T | CA398751701 | HNF1B | c.371T>A (p.Met124Lys) | |
17 | g.37739614T>A | CA398751702 | HNF1B | c.370A>T (p.Met124Leu) | |
17 | g.37739614T>C | CA398751703 | HNF1B | c.370A>G (p.Met124Val) | |
17 | g.37739614T>G | CA398751704 | HNF1B | c.370A>C (p.Met124Leu) | |
17 | g.37739617del | CA2695196522 | HNF1B | c.370del (p.Met124Ter) | |
17 | g.37739615T>A | CA398751705 | HNF1B | c.369A>T (p.Lys123Asn) | |
17 | g.37739615T>C | CA499603976 | HNF1B | c.369A>G (p.Lys123=) | |
17 | g.37739615T>G | CA398751706 | HNF1B | c.369A>C (p.Lys123Asn) | |
17 | g.37739616T>A | CA398751707 | HNF1B | c.368A>T (p.Lys123Ile) | |
17 | g.37739616T>C | CA398751708 | HNF1B | c.368A>G (p.Lys123Arg) | |
17 | g.37739616T>G | CA398751709 | HNF1B | c.368A>C (p.Lys123Thr) | |
17 | g.37739617T>A | CA398751710 | HNF1B | c.367A>T (p.Lys123Ter) | |
17 | g.37739617T>C | CA398751711 | HNF1B | c.367A>G (p.Lys123Glu) | |
17 | g.37739617T>G | CA398751712 | HNF1B | c.367A>C (p.Lys123Gln) |