Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.37739503_37739577del | CA913190793 | HNF1B | c.410_484del (p.Arg137_Lys161del) | ClinVar |
17 | g.37739547T>A | CA398751458 | HNF1B | c.437A>T (p.Asn146Ile) | |
17 | g.37739547T>C | CA398751455 | HNF1B | c.437A>G (p.Asn146Ser) | |
17 | g.37739547T>G | CA398751457 | HNF1B | c.437A>C (p.Asn146Thr) | ClinVar |
17 | g.37739548T>A | CA398751460 | HNF1B | c.436A>T (p.Asn146Tyr) | |
17 | g.37739548T>C | CA398751462 | HNF1B | c.436A>G (p.Asn146Asp) | ClinVar |
17 | g.37739548T>G | CA398751464 | HNF1B | c.436A>C (p.Asn146His) | |
17 | g.37739549C>A | CA499603942 | HNF1B | c.435G>T (p.Leu145=) | |
17 | g.37739549C>G | CA499603940 | HNF1B | c.435G>C (p.Leu145=) | |
17 | g.37739549C>T | CA499603941 | HNF1B | c.435G>A (p.Leu145=) | |
17 | g.37739550del | CA2695225794 | HNF1B | c.434del (p.Leu145ArgfsTer16) | |
17 | g.37739550A>C | CA398751465 | HNF1B | c.434T>G (p.Leu145Arg) | |
17 | g.37739550A>G | CA398751466 | HNF1B | c.434T>C (p.Leu145Pro) | |
17 | g.37739550A>T | CA398751468 | HNF1B | c.434T>A (p.Leu145Gln) | ClinVar |
17 | g.37739551G>A | CA499603943 | HNF1B | c.433C>T (p.Leu145=) | |
17 | g.37739551G>C | CA398751470 | HNF1B | c.433C>G (p.Leu145Val) | |
17 | g.37739551G>T | CA398751471 | HNF1B | c.433C>A (p.Leu145Met) | |
17 | g.37739552G>A | CA499603946 | HNF1B | c.432C>T (p.Gly144=) | dbSNP |
17 | g.37739552G>C | CA499603945 | HNF1B | c.432C>G (p.Gly144=) | |
17 | g.37739552G>T | CA499603944 | HNF1B | c.432C>A (p.Gly144=) | |
17 | g.37739553C>A | CA398751472 | HNF1B | c.431G>T (p.Gly144Val) | dbSNP |
17 | g.37739553C>G | CA398751474 | HNF1B | c.431G>C (p.Gly144Ala) | |
17 | g.37739553C>T | CA398751475 | HNF1B | c.431G>A (p.Gly144Asp) | |
17 | g.37739554C>A | CA398751480 | HNF1B | c.430G>T (p.Gly144Cys) | |
17 | g.37739554C>G | CA398751478 | HNF1B | c.430G>C (p.Gly144Arg) | |
17 | g.37739554C>T | CA8519075 | HNF1B | c.430G>A (p.Gly144Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739555G>A | CA8519076 | HNF1B | c.429C>T (p.Thr143=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739555G>C | CA499603947 | HNF1B | c.429C>G (p.Thr143=) | |
17 | g.37739555G>T | CA499603948 | HNF1B | c.429C>A (p.Thr143=) | |
17 | g.37739556G>A | CA398751485 | HNF1B | c.428C>T (p.Thr143Ile) | |
17 | g.37739556G>C | CA398751482 | HNF1B | c.428C>G (p.Thr143Ser) | |
17 | g.37739556G>T | CA398751483 | HNF1B | c.428C>A (p.Thr143Asn) | |
17 | g.37739557T>A | CA398751487 | HNF1B | c.427A>T (p.Thr143Ser) | |
17 | g.37739557T>C | CA398751488 | HNF1B | c.427A>G (p.Thr143Ala) | |
17 | g.37739557T>G | CA398751490 | HNF1B | c.427A>C (p.Thr143Pro) | |
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) | |
17 | g.37739574C>G | CA398751551 | HNF1B | c.410G>C (p.Arg137Thr) | |
17 | g.37739574C>T | CA398751552 | HNF1B | c.410G>A (p.Arg137Lys) | ClinVar dbSNP gnomAD v4 |
17 | g.37739575T>A | CA398751554 | HNF1B | c.409A>T (p.Arg137Trp) | |
17 | g.37739575T>C | CA398751555 | HNF1B | c.409A>G (p.Arg137Gly) | |
17 | g.37739575T>G | CA499603960 | HNF1B | c.409A>C (p.Arg137=) | |
17 | g.37739576C>A | CA398751557 | HNF1B | c.408G>T (p.Gln136His) | |
17 | g.37739576C>G | CA398751559 | HNF1B | c.408G>C (p.Gln136His) | |
17 | g.37739576C>T | CA499603961 | HNF1B | c.408G>A (p.Gln136=) | |
17 | g.37739577T>A | CA398751561 | HNF1B | c.407A>T (p.Gln136Leu) | |
17 | g.37739577T>C | CA398751562 | HNF1B | c.407A>G (p.Gln136Arg) | |
17 | g.37739577T>G | CA398751564 | HNF1B | c.407A>C (p.Gln136Pro) | |
17 | g.37739578G>A | CA398751565 | HNF1B | c.406C>T (p.Gln136Ter) | ClinVar |
17 | g.37739578G>C | CA398751567 | HNF1B | c.406C>G (p.Gln136Glu) | ClinVar |
17 | g.37739578G>T | CA398751568 | HNF1B | c.406C>A (p.Gln136Lys) | |
17 | g.37739582dup | CA10603444 | HNF1B | c.406dup (p.Gln136ProfsTer?) | ClinVar dbSNP |
17 | g.37739579G>A | CA499603962 | HNF1B | c.405C>T (p.Pro135=) | |
17 | g.37739579G>C | CA499603963 | HNF1B | c.405C>G (p.Pro135=) | |
17 | g.37739579G>T | CA499603964 | HNF1B | c.405C>A (p.Pro135=) | |
17 | g.37739580G>A | CA398751570 | HNF1B | c.404C>T (p.Pro135Leu) | |
17 | g.37739580G>C | CA398751572 | HNF1B | c.404C>G (p.Pro135Arg) | |
17 | g.37739580G>T | CA398751573 | HNF1B | c.404C>A (p.Pro135His) | |
17 | g.37739581G>A | CA398751578 | HNF1B | c.403C>T (p.Pro135Ser) | |
17 | g.37739581G>C | CA398751577 | HNF1B | c.403C>G (p.Pro135Ala) | |
17 | g.37739581G>T | CA398751575 | HNF1B | c.403C>A (p.Pro135Thr) | |
17 | g.37739582G>A | CA499603965 | HNF1B | c.402C>T (p.Ile134=) | ClinVar dbSNP gnomAD v4 |
17 | g.37739582G>C | CA398751580 | HNF1B | c.402C>G (p.Ile134Met) | |
17 | g.37739582G>T | CA499603966 | HNF1B | c.402C>A (p.Ile134=) | gnomAD v4 |
17 | g.37739583A>C | CA398751585 | HNF1B | c.401T>G (p.Ile134Ser) | |
17 | g.37739583A>G | CA398751582 | HNF1B | c.401T>C (p.Ile134Thr) | |
17 | g.37739583A>T | CA398751583 | HNF1B | c.401T>A (p.Ile134Asn) | ClinVar dbSNP |
17 | g.37739584T>A | CA398751587 | HNF1B | c.400A>T (p.Ile134Phe) | |
17 | g.37739584T>C | CA398751589 | HNF1B | c.400A>G (p.Ile134Val) | |
17 | g.37739584T>G | CA398751590 | HNF1B | c.400A>C (p.Ile134Leu) | |
17 | g.37739585G>A | CA499603967 | HNF1B | c.399C>T (p.Asn133=) | dbSNP |
17 | g.37739585G>C | CA398751591 | HNF1B | c.399C>G (p.Asn133Lys) | |
17 | g.37739585G>T | CA398751593 | HNF1B | c.399C>A (p.Asn133Lys) | |
17 | g.37739586T>A | CA398751595 | HNF1B | c.398A>T (p.Asn133Ile) | |
17 | g.37739586T>C | CA398751597 | HNF1B | c.398A>G (p.Asn133Ser) | ClinVar |
17 | g.37739586T>G | CA398751598 | HNF1B | c.398A>C (p.Asn133Thr) | |
17 | g.37739587T>A | CA398751600 | HNF1B | c.397A>T (p.Asn133Tyr) | |
17 | g.37739587T>C | CA398751601 | HNF1B | c.397A>G (p.Asn133Asp) | |
17 | g.37739587T>G | CA398751603 | HNF1B | c.397A>C (p.Asn133His) | |
17 | g.37739588G>A | CA499603968 | HNF1B | c.396C>T (p.His132=) | |
17 | g.37739588G>C | CA398751604 | HNF1B | c.396C>G (p.His132Gln) | dbSNP |
17 | g.37739588G>T | CA398751606 | HNF1B | c.396C>A (p.His132Gln) | |
17 | g.37739589T>A | CA398751607 | HNF1B | c.395A>T (p.His132Leu) | |
17 | g.37739589T>C | CA398751609 | HNF1B | c.395A>G (p.His132Arg) | ClinVar |
17 | g.37739589T>G | CA398751611 | HNF1B | c.395A>C (p.His132Pro) | ClinVar |
17 | g.37739591_37739596del | CA2695225795 | HNF1B | c.390_395del (p.Gln130_Gln131del) | |
17 | g.37739590G>A | CA398751612 | HNF1B | c.394C>T (p.His132Tyr) | gnomAD v4 |
17 | g.37739590G>C | CA398751613 | HNF1B | c.394C>G (p.His132Asp) | |
17 | g.37739590G>T | CA398751615 | HNF1B | c.394C>A (p.His132Asn) | |
17 | g.37739591T>A | CA398751616 | HNF1B | c.393A>T (p.Gln131His) | |
17 | g.37739591T>C | CA499603969 | HNF1B | c.393A>G (p.Gln131=) | |
17 | g.37739591T>G | CA398751617 | HNF1B | c.393A>C (p.Gln131His) | |
17 | g.37739592T>A | CA398751619 | HNF1B | c.392A>T (p.Gln131Leu) | |
17 | g.37739592T>C | CA398751620 | HNF1B | c.392A>G (p.Gln131Arg) | |
17 | g.37739592T>G | CA398751622 | HNF1B | c.392A>C (p.Gln131Pro) | |
17 | g.37739594_37739600del | CA913190796 | HNF1B | c.386_392del (p.Met129AsnfsTer15) | ClinVar |
17 | g.37739593G>A | CA398751625 | HNF1B | c.391C>T (p.Gln131Ter) | ClinVar |
17 | g.37739593G>C | CA398751626 | HNF1B | c.391C>G (p.Gln131Glu) | |
17 | g.37739593G>T | CA398751624 | HNF1B | c.391C>A (p.Gln131Lys) | |
17 | g.37739594C>A | CA398751628 | HNF1B | c.390G>T (p.Gln130His) | |
17 | g.37739594C>G | CA398751629 | HNF1B | c.390G>C (p.Gln130His) | |
17 | g.37739594C>T | CA499603970 | HNF1B | c.390G>A (p.Gln130=) | |
17 | g.37739595T>A | CA398751632 | HNF1B | c.389A>T (p.Gln130Leu) | |
17 | g.37739595T>C | CA398751633 | HNF1B | c.389A>G (p.Gln130Arg) | |
17 | g.37739595T>G | CA398751634 | HNF1B | c.389A>C (p.Gln130Pro) | |
17 | g.37739596G>A | CA398751640 | HNF1B | c.388C>T (p.Gln130Ter) | |
17 | g.37739596G>C | CA398751638 | HNF1B | c.388C>G (p.Gln130Glu) | |
17 | g.37739596G>T | CA398751636 | HNF1B | c.388C>A (p.Gln130Lys) | |
17 | g.37739597C>A | CA398751641 | HNF1B | c.387G>T (p.Met129Ile) | |
17 | g.37739597C>G | CA398751643 | HNF1B | c.387G>C (p.Met129Ile) | gnomAD v4 |
17 | g.37739597C>T | CA398751645 | HNF1B | c.387G>A (p.Met129Ile) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739598A>C | CA398751647 | HNF1B | c.386T>G (p.Met129Arg) | |
17 | g.37739598A>G | CA398751648 | HNF1B | c.386T>C (p.Met129Thr) | |
17 | g.37739598A>T | CA398751649 | HNF1B | c.386T>A (p.Met129Lys) | |
17 | g.37739599T>A | CA398751651 | HNF1B | c.385A>T (p.Met129Leu) | |
17 | g.37739599T>C | CA398751654 | HNF1B | c.385A>G (p.Met129Val) | |
17 | g.37739599T>G | CA398751653 | HNF1B | c.385A>C (p.Met129Leu) | |
17 | g.37739600G>A | CA499603971 | HNF1B | c.384C>T (p.Tyr128=) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739600G>C | CA398751656 | HNF1B | c.384C>G (p.Tyr128Ter) | |
17 | g.37739600G>T | CA398751658 | HNF1B | c.384C>A (p.Tyr128Ter) | |
17 | g.37739601T>A | CA398751659 | HNF1B | c.383A>T (p.Tyr128Phe) | dbSNP |
17 | g.37739601T>C | CA398751660 | HNF1B | c.383A>G (p.Tyr128Cys) | |
17 | g.37739601T>G | CA398751661 | HNF1B | c.383A>C (p.Tyr128Ser) | |
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) | |
17 | g.37739618A>C | CA499603977 | HNF1B | c.366T>G (p.Ala122=) | |
17 | g.37739618A>G | CA499603978 | HNF1B | c.366T>C (p.Ala122=) | dbSNP |
17 | g.37739618A>T | CA499603979 | HNF1B | c.366T>A (p.Ala122=) | |
17 | g.37739619G>A | CA398751714 | HNF1B | c.365C>T (p.Ala122Val) | |
17 | g.37739619G>C | CA398751715 | HNF1B | c.365C>G (p.Ala122Gly) | |
17 | g.37739619G>T | CA398751713 | HNF1B | c.365C>A (p.Ala122Asp) | |
17 | g.37739620C>A | CA398751716 | HNF1B | c.364G>T (p.Ala122Ser) | |
17 | g.37739620C>G | CA398751717 | HNF1B | c.364G>C (p.Ala122Pro) | |
17 | g.37739620C>T | CA398751718 | HNF1B | c.364G>A (p.Ala122Thr) | ClinVar dbSNP |
17 | g.37739621A>C | CA499603982 | HNF1B | c.363T>G (p.Ala121=) | |
17 | g.37739621A>G | CA499603981 | HNF1B | c.363T>C (p.Ala121=) | |
17 | g.37739621A>T | CA499603980 | HNF1B | c.363T>A (p.Ala121=) | |
17 | g.37739622G>A | CA398751719 | HNF1B | c.362C>T (p.Ala121Val) | |
17 | g.37739622G>C | CA398751720 | HNF1B | c.362C>G (p.Ala121Gly) | |
17 | g.37739622G>T | CA398751721 | HNF1B | c.362C>A (p.Ala121Asp) | |
17 | g.37739623C>A | CA398751722 | HNF1B | c.361G>T (p.Ala121Ser) | |
17 | g.37739623C>G | CA398751723 | HNF1B | c.361G>C (p.Ala121Pro) | |
17 | g.37739623C>T | CA398751724 | HNF1B | c.361G>A (p.Ala121Thr) | gnomAD v4 |
17 | g.37739624C>A | CA398751725 | HNF1B | c.360G>T (p.Arg120Ser) | |
17 | g.37739624C>G | CA398751726 | HNF1B | c.360G>C (p.Arg120Ser) | |
17 | g.37739624C>T | CA499603983 | HNF1B | c.360G>A (p.Arg120=) | |
17 | g.37739625C>A | CA398751729 | HNF1B | c.359G>T (p.Arg120Met) | |
17 | g.37739625C>G | CA398751728 | HNF1B | c.359G>C (p.Arg120Thr) | |
17 | g.37739625C>T | CA398751727 | HNF1B | c.359G>A (p.Arg120Lys) | |
17 | g.37739626T>A | CA398751730 | HNF1B | c.358A>T (p.Arg120Trp) | |
17 | g.37739626T>C | CA398751731 | HNF1B | c.358A>G (p.Arg120Gly) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739626T>G | CA499603984 | HNF1B | c.358A>C (p.Arg120=) | |
17 | g.37739627C>A | CA398751732 | HNF1B | c.357G>T (p.Trp119Cys) | |
17 | g.37739627C>G | CA398751733 | HNF1B | c.357G>C (p.Trp119Cys) | |
17 | g.37739627C>T | CA398751734 | HNF1B | c.357G>A (p.Trp119Ter) | |
17 | g.37739628C>A | CA398751735 | HNF1B | c.356G>T (p.Trp119Leu) | |
17 | g.37739628C>G | CA398751736 | HNF1B | c.356G>C (p.Trp119Ser) | |
17 | g.37739628C>T | CA398751737 | HNF1B | c.356G>A (p.Trp119Ter) | ClinVar |
17 | g.37739629A>C | CA398751738 | HNF1B | c.355T>G (p.Trp119Gly) | |
17 | g.37739629A>G | CA398751739 | HNF1B | c.355T>C (p.Trp119Arg) | |
17 | g.37739629A>T | CA398751740 | HNF1B | c.355T>A (p.Trp119Arg) | |
17 | g.37739630A>C | CA499603985 | HNF1B | c.354T>G (p.Pro118=) | |
17 | g.37739630A>G | CA8519080 | HNF1B | c.354T>C (p.Pro118=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739630A>T | CA499603986 | HNF1B | c.354T>A (p.Pro118=) | |
17 | g.37739631G>A | CA398751743 | HNF1B | c.353C>T (p.Pro118Leu) | |
17 | g.37739631G>C | CA398751742 | HNF1B | c.353C>G (p.Pro118Arg) | |
17 | g.37739631G>T | CA398751741 | HNF1B | c.353C>A (p.Pro118His) | gnomAD v3 gnomAD v4 |
17 | g.37739633del | CA913190797 | HNF1B | c.353del (p.Pro118LeufsTer7) | ClinVar |
17 | g.37739632G>A | CA398751744 | HNF1B | c.352C>T (p.Pro118Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739632G>C | CA398751745 | HNF1B | c.352C>G (p.Pro118Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739632G>T | CA8519081 | HNF1B | c.352C>A (p.Pro118Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739633G>A | CA499603987 | HNF1B | c.351C>T (p.Asp117=) | gnomAD v4 |
17 | g.37739633G>C | CA398751746 | HNF1B | c.351C>G (p.Asp117Glu) | |
17 | g.37739633G>T | CA398751747 | HNF1B | c.351C>A (p.Asp117Glu) | |
17 | g.37739634T>A | CA290288735 | HNF1B | c.350A>T (p.Asp117Val) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739634T>C | CA398751748 | HNF1B | c.350A>G (p.Asp117Gly) | |
17 | g.37739634T>G | CA398751749 | HNF1B | c.350A>C (p.Asp117Ala) | |
17 | g.37739635C>A | CA398751750 | HNF1B | c.349G>T (p.Asp117Tyr) | |
17 | g.37739635C>G | CA398751751 | HNF1B | c.349G>C (p.Asp117His) | |
17 | g.37739635C>T | CA398751752 | HNF1B | c.349G>A (p.Asp117Asn) | |
17 | g.37739636C>A | CA398751753 | HNF1B | c.348G>T (p.Glu116Asp) | gnomAD v4 |
17 | g.37739636C>G | CA398751754 | HNF1B | c.348G>C (p.Glu116Asp) | |
17 | g.37739636C>T | CA499603988 | HNF1B | c.348G>A (p.Glu116=) | |
17 | g.37739637T>A | CA398751755 | HNF1B | c.347A>T (p.Glu116Val) | gnomAD v4 |
17 | g.37739637T>C | CA398751756 | HNF1B | c.347A>G (p.Glu116Gly) | |
17 | g.37739637T>G | CA398751757 | HNF1B | c.347A>C (p.Glu116Ala) | |
17 | g.37739638C>A | CA398751758 | HNF1B | c.346G>T (p.Glu116Ter) | |
17 | g.37739638C>G | CA398751760 | HNF1B | c.346G>C (p.Glu116Gln) | |
17 | g.37739638C>T | CA398751759 | HNF1B | c.346G>A (p.Glu116Lys) | |
17 | g.37739639A>C | CA398751761 | HNF1B | c.345T>G (p.Ser115Arg) | |
17 | g.37739639A>G | CA499603992 | HNF1B | c.345T>C (p.Ser115=) | |
17 | g.37739639A>T | CA398751762 | HNF1B | c.345T>A (p.Ser115Arg) | |
17 | g.37739640C>A | CA214359 | HNF1B | c.345-1G>T (n.345-1G>T) | ClinVar dbSNP |
17 | g.37739640C>G | CA398751763 | HNF1B | c.345-1G>C (n.345-1G>C) | |
17 | g.37739640C>T | CA398751764 | HNF1B | c.345-1G>A (n.345-1G>A) | ClinVar |
17 | g.37739641T>A | CA398751765 | HNF1B | c.345-2A>T (n.345-2A>T) | |
17 | g.37739641T>C | CA398751766 | HNF1B | c.345-2A>G (n.345-2A>G) | ClinVar |
17 | g.37739641T>G | CA398751767 | HNF1B | c.345-2A>C (n.345-2A>C) | |
17 | g.37739643G>A | CA8519082 | HNF1B | c.345-4C>T (n.345-4C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739643G>C | CA626207311 | HNF1B | c.345-4C>G (n.345-4C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739643G>T | CA2637449190 | HNF1B | c.345-4C>A (n.345-4C>A) | gnomAD v4 |
17 | g.37739644A>G | CA2576244088 | HNF1B | c.345-5T>C (n.345-5T>C) | |
17 | g.37739645C>G | CA290288748 | HNF1B | c.345-6G>C (n.345-6G>C) | dbSNP |
17 | g.37739646_37739647insAA | CA626207312 | HNF1B | c.345-7_345-6insTT (n.345-7_345-6insTT) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739647G>C | CA2739267525 | HNF1B | c.345-8C>G (n.345-8C>G) | ClinVar |