| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739503_37739577del | CA913190793 | HNF1B | c.410_484del (p.Arg137_Lys161del) | ClinVar |
| 17 | g.37739558G>A | CA499603949 | HNF1B | c.426C>T (p.Val142=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.37739558G>C | CA499603950 | HNF1B | c.426C>G (p.Val142=) | |
| 17 | g.37739558G>T | CA499603951 | HNF1B | c.426C>A (p.Val142=) | |
| 17 | g.37739559A>C | CA398751493 | HNF1B | c.425T>G (p.Val142Gly) | |
| 17 | g.37739559A>G | CA398751494 | HNF1B | c.425T>C (p.Val142Ala) | |
| 17 | g.37739559A>T | CA398751495 | HNF1B | c.425T>A (p.Val142Asp) | |
| 17 | g.37739560C>A | CA398751497 | HNF1B | c.424G>T (p.Val142Phe) | |
| 17 | g.37739560C>G | CA398751499 | HNF1B | c.424G>C (p.Val142Leu) | |
| 17 | g.37739560C>T | CA398751502 | HNF1B | c.424G>A (p.Val142Ile) | |
| 17 | g.37739561A>C | CA398751504 | HNF1B | c.423T>G (p.Asp141Glu) | |
| 17 | g.37739561A>G | CA499603952 | HNF1B | c.423T>C (p.Asp141=) | dbSNP |
| 17 | g.37739561A>T | CA398751505 | HNF1B | c.423T>A (p.Asp141Glu) | |
| 17 | g.37739562T>A | CA398751508 | HNF1B | c.422A>T (p.Asp141Val) | |
| 17 | g.37739562T>C | CA398751507 | HNF1B | c.422A>G (p.Asp141Gly) | |
| 17 | g.37739562T>G | CA398751506 | HNF1B | c.422A>C (p.Asp141Ala) | |
| 17 | g.37739563C>A | CA398751510 | HNF1B | c.421G>T (p.Asp141Tyr) | |
| 17 | g.37739563C>G | CA398751512 | HNF1B | c.421G>C (p.Asp141His) | |
| 17 | g.37739563C>T | CA290288699 | HNF1B | c.421G>A (p.Asp141Asn) | dbSNP gnomAD v4 |
| 17 | g.37739564G>A | CA8519077 | HNF1B | c.420C>T (p.Val140=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.37739564G>C | CA499603953 | HNF1B | c.420C>G (p.Val140=) | |
| 17 | g.37739564G>T | CA499603954 | HNF1B | c.420C>A (p.Val140=) | |
| 17 | g.37739565A>C | CA398751514 | HNF1B | c.419T>G (p.Val140Gly) | |
| 17 | g.37739565A>G | CA398751515 | HNF1B | c.419T>C (p.Val140Ala) | |
| 17 | g.37739565A>T | CA398751516 | HNF1B | c.419T>A (p.Val140Asp) | |
| 17 | g.37739566C>A | CA398751519 | HNF1B | c.418G>T (p.Val140Phe) | gnomAD v4 |
| 17 | g.37739566C>G | CA398751520 | HNF1B | c.418G>C (p.Val140Leu) | |
| 17 | g.37739566C>T | CA398751522 | HNF1B | c.418G>A (p.Val140Ile) | |
| 17 | g.37739567C>A | CA499603955 | HNF1B | c.417G>T (p.Val139=) | |
| 17 | g.37739567C>G | CA499603956 | HNF1B | c.417G>C (p.Val139=) | |
| 17 | g.37739567C>T | CA499603957 | HNF1B | c.417G>A (p.Val139=) | |
| 17 | g.37739568A>C | CA398751523 | HNF1B | c.416T>G (p.Val139Gly) | ClinVar |
| 17 | g.37739568A>G | CA398751525 | HNF1B | c.416T>C (p.Val139Ala) | gnomAD v4 |
| 17 | g.37739568A>T | CA398751528 | HNF1B | c.416T>A (p.Val139Glu) | |
| 17 | g.37739569C>A | CA398751532 | HNF1B | c.415G>T (p.Val139Leu) | |
| 17 | g.37739569C>G | CA398751534 | HNF1B | c.415G>C (p.Val139Leu) | |
| 17 | g.37739569C>T | CA398751530 | HNF1B | c.415G>A (p.Val139Met) | |
| 17 | g.37739570C>A | CA398751536 | HNF1B | c.414G>T (p.Glu138Asp) | |
| 17 | g.37739570C>G | CA398751537 | HNF1B | c.414G>C (p.Glu138Asp) | |
| 17 | g.37739570C>T | CA499603958 | HNF1B | c.414G>A (p.Glu138=) | |
| 17 | g.37739571T>A | CA398751538 | HNF1B | c.413A>T (p.Glu138Val) | |
| 17 | g.37739571T>C | CA398751539 | HNF1B | c.413A>G (p.Glu138Gly) | |
| 17 | g.37739571T>G | CA398751540 | HNF1B | c.413A>C (p.Glu138Ala) | |
| 17 | g.37739572C>A | CA398751541 | HNF1B | c.412G>T (p.Glu138Ter) | |
| 17 | g.37739572C>G | CA398751543 | HNF1B | c.412G>C (p.Glu138Gln) | |
| 17 | g.37739572C>T | CA398751545 | HNF1B | c.412G>A (p.Glu138Lys) | |
| 17 | g.37739573C>A | CA398751546 | HNF1B | c.411G>T (p.Arg137Ser) | |
| 17 | g.37739573C>G | CA398751548 | HNF1B | c.411G>C (p.Arg137Ser) | |
| 17 | g.37739573C>T | CA499603959 | HNF1B | c.411G>A (p.Arg137=) | |
| 17 | g.37739574C>A | CA398751549 | HNF1B | c.410G>T (p.Arg137Met) |