UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.44305065G>A | CA359697620 | FGF10 | c.557C>T (p.Pro186Leu) | |
| 5 | g.44305065G>C | CA359697619 | FGF10 | c.557C>G (p.Pro186Arg) | |
| 5 | g.44305065G>T | CA359697618 | FGF10 | c.557C>A (p.Pro186Gln) | COSMIC |
| 5 | g.44305066G>A | CA359697621 | FGF10 | c.556C>T (p.Pro186Ser) | |
| 5 | g.44305066G>C | CA359697622 | FGF10 | c.556C>G (p.Pro186Ala) | |
| 5 | g.44305066G>T | CA359697623 | FGF10 | c.556C>A (p.Pro186Thr) | |
| 5 | g.44305067A>C | CA444230909 | FGF10 | c.555T>G (p.Ala185=) | |
| 5 | g.44305067A>G | CA444230911 | FGF10 | c.555T>C (p.Ala185=) | |
| 5 | g.44305067A>T | CA444230910 | FGF10 | c.555T>A (p.Ala185=) | |
| 5 | g.44305068G>A | CA118160546 | FGF10 | c.554C>T (p.Ala185Val) | dbSNP |
| 5 | g.44305068G>C | CA359697624 | FGF10 | c.554C>G (p.Ala185Gly) | |
| 5 | g.44305068G= | CA1543079523 | FGF10 | c.554C= (p.Ala185=) | |
| 5 | g.44305068G>T | CA359697625 | FGF10 | c.554C>A (p.Ala185Asp) | |
| 5 | g.44305069C>A | CA359697626 | FGF10 | c.553G>T (p.Ala185Ser) | |
| 5 | g.44305069C= | CA1543079528 | FGF10 | c.553G= (p.Ala185=) | |
| 5 | g.44305069C>G | CA359697627 | FGF10 | c.553G>C (p.Ala185Pro) | |
| 5 | g.44305069C>T | CA359697628 | FGF10 | c.553G>A (p.Ala185Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.44305070T>A | CA444230912 | FGF10 | c.552A>T (p.Gly184=) | |
| 5 | g.44305070T>C | CA444230913 | FGF10 | c.552A>G (p.Gly184=) | gnomAD v4 |
| 5 | g.44305070T>G | CA444230914 | FGF10 | c.552A>C (p.Gly184=) | gnomAD v4 |
| 5 | g.44305071C>A | CA359697629 | FGF10 | c.551G>T (p.Gly184Val) | |
| 5 | g.44305071C>G | CA359697630 | FGF10 | c.551G>C (p.Gly184Ala) | |
| 5 | g.44305071C>T | CA359697631 | FGF10 | c.551G>A (p.Gly184Glu) | dbSNP |
| 5 | g.44305072C>A | CA359697634 | FGF10 | c.550G>T (p.Gly184Ter) | COSMIC |
| 5 | g.44305072C= | CA1543079532 | FGF10 | c.550G= (p.Gly184=) | |
| 5 | g.44305072C>G | CA359697632 | FGF10 | c.550G>C (p.Gly184Arg) | |
| 5 | g.44305072C>T | CA359697633 | FGF10 | c.550G>A (p.Gly184Arg) | ClinVar dbSNP COSMIC |
| 5 | g.44305073T>A | CA359697635 | FGF10 | c.549A>T (p.Lys183Asn) | |
| 5 | g.44305073T>C | CA444230916 | FGF10 | c.549A>G (p.Lys183=) | dbSNP |
| 5 | g.44305073T>G | CA359697636 | FGF10 | c.549A>C (p.Lys183Asn) | |
| 5 | g.44305076del | CA2708817182 | FGF10 | c.549del (p.Gly184GlufsTer?) | dbSNP |
| 5 | g.44305074T>A | CA359697637 | FGF10 | c.548A>T (p.Lys183Ile) | |
| 5 | g.44305074T>C | CA118160547 | FGF10 | c.548A>G (p.Lys183Arg) | dbSNP gnomAD v4 |
| 5 | g.44305074T>G | CA359697638 | FGF10 | c.548A>C (p.Lys183Thr) | |
| 5 | g.44305074T= | CA1543079535 | FGF10 | c.548A= (p.Lys183=) | |
| 5 | g.44305075T>A | CA359697639 | FGF10 | c.547A>T (p.Lys183Ter) | |
| 5 | g.44305075T>C | CA359697640 | FGF10 | c.547A>G (p.Lys183Glu) | |
| 5 | g.44305075T>G | CA359697641 | FGF10 | c.547A>C (p.Lys183Gln) | |
| 5 | g.44305076T>A | CA444230917 | FGF10 | c.546A>T (p.Gly182=) | |
| 5 | g.44305076T>C | CA444230918 | FGF10 | c.546A>G (p.Gly182=) | |
| 5 | g.44305076T>G | CA444230919 | FGF10 | c.546A>C (p.Gly182=) | |
| 5 | g.44305077C>A | CA359697642 | FGF10 | c.545G>T (p.Gly182Val) | |
| 5 | g.44305077C>G | CA359697643 | FGF10 | c.545G>C (p.Gly182Ala) | |
| 5 | g.44305077C>T | CA359697644 | FGF10 | c.545G>A (p.Gly182Glu) | |
| 5 | g.44305078C>A | CA359697647 | FGF10 | c.544G>T (p.Gly182Ter) | COSMIC |
| 5 | g.44305078C>G | CA359697646 | FGF10 | c.544G>C (p.Gly182Arg) | |
| 5 | g.44305078C>T | CA359697645 | FGF10 | c.544G>A (p.Gly182Arg) | COSMIC |
| 5 | g.44305079A= | CA1543079539 | FGF10 | c.543T= (p.Asn181=) | |
| 5 | g.44305079A>C | CA359697648 | FGF10 | c.543T>G (p.Asn181Lys) | gnomAD v4 |
| 5 | g.44305079A>G | CA118160548 | FGF10 | c.543T>C (p.Asn181=) | dbSNP gnomAD v4 |
| 5 | g.44305079A>T | CA359697649 | FGF10 | c.543T>A (p.Asn181Lys) | |
| 5 | g.44305080T>A | CA359697650 | FGF10 | c.542A>T (p.Asn181Ile) | |
| 5 | g.44305080T>C | CA359697651 | FGF10 | c.542A>G (p.Asn181Ser) | |
| 5 | g.44305080T>G | CA359697652 | FGF10 | c.542A>C (p.Asn181Thr) | |
| 5 | g.44305081T>A | CA359697653 | FGF10 | c.541A>T (p.Asn181Tyr) | |
| 5 | g.44305081T>C | CA359697654 | FGF10 | c.541A>G (p.Asn181Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.44305081T>G | CA359697655 | FGF10 | c.541A>C (p.Asn181His) | ClinVar dbSNP |
| 5 | g.44305081T= | CA1543079543 | FGF10 | c.541A= (p.Asn181=) | |
| 5 | g.44305082C>A | CA359697656 | FGF10 | c.540G>T (p.Leu180Phe) | |
| 5 | g.44305082C>G | CA359697657 | FGF10 | c.540G>C (p.Leu180Phe) | |
| 5 | g.44305082C>T | CA444230920 | FGF10 | c.540G>A (p.Leu180=) | |
| 5 | g.44305083A>C | CA359697658 | FGF10 | c.539T>G (p.Leu180Trp) | |
| 5 | g.44305083A>G | CA359697659 | FGF10 | c.539T>C (p.Leu180Ser) | ClinVar gnomAD v4 |
| 5 | g.44305083A>T | CA359697660 | FGF10 | c.539T>A (p.Leu180Ter) | |
| 5 | g.44305084A>C | CA359697661 | FGF10 | c.538T>G (p.Leu180Val) | |
| 5 | g.44305084A>G | CA444230921 | FGF10 | c.538T>C (p.Leu180=) | |
| 5 | g.44305084A>T | CA359697662 | FGF10 | c.538T>A (p.Leu180Met) | |
| 5 | g.44305085T>A | CA444230922 | FGF10 | c.537A>T (p.Ala179=) | |
| 5 | g.44305085T>C | CA444230923 | FGF10 | c.537A>G (p.Ala179=) | gnomAD v4 |
| 5 | g.44305085T>G | CA444230924 | FGF10 | c.537A>C (p.Ala179=) | |
| 5 | g.44305086G>A | CA359697663 | FGF10 | c.536C>T (p.Ala179Val) | |
| 5 | g.44305086G>C | CA359697665 | FGF10 | c.536C>G (p.Ala179Gly) | |
| 5 | g.44305086G>T | CA359697664 | FGF10 | c.536C>A (p.Ala179Glu) | |
| 5 | g.44305087C>A | CA118160549 | FGF10 | c.535G>T (p.Ala179Ser) | dbSNP |
| 5 | g.44305087C= | CA1543079551 | FGF10 | c.535G= (p.Ala179=) | |
| 5 | g.44305087C>G | CA359697666 | FGF10 | c.535G>C (p.Ala179Pro) | |
| 5 | g.44305087C>T | CA359697667 | FGF10 | c.535G>A (p.Ala179Thr) | gnomAD v4 |
| 5 | g.44305088C>A | CA444230925 | FGF10 | c.534G>T (p.Val178=) | |
| 5 | g.44305088C= | CA1543079559 | FGF10 | c.534G= (p.Val178=) | |
| 5 | g.44305088C>G | CA444230926 | FGF10 | c.534G>C (p.Val178=) | |
| 5 | g.44305088C>T | CA3258483 | FGF10 | c.534G>A (p.Val178=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.44305089A>C | CA359697668 | FGF10 | c.533T>G (p.Val178Gly) | |
| 5 | g.44305089A>G | CA359697669 | FGF10 | c.533T>C (p.Val178Ala) | gnomAD v4 |
| 5 | g.44305089A>T | CA359697670 | FGF10 | c.533T>A (p.Val178Glu) | |
| 5 | g.44305090C>A | CA359697671 | FGF10 | c.532G>T (p.Val178Leu) | |
| 5 | g.44305090C= | CA1543079576 | FGF10 | c.532G= (p.Val178=) | |
| 5 | g.44305090C>G | CA359697672 | FGF10 | c.532G>C (p.Val178Leu) | |
| 5 | g.44305090C>T | CA359697673 | FGF10 | c.532G>A (p.Val178Met) | dbSNP |
| 5 | g.44305091A>C | CA359697674 | FGF10 | c.531T>G (p.Tyr177Ter) | |
| 5 | g.44305091A>G | CA444230927 | FGF10 | c.531T>C (p.Tyr177=) | gnomAD v4 |
| 5 | g.44305091A>T | CA359697675 | FGF10 | c.531T>A (p.Tyr177Ter) | |
| 5 | g.44305092T>A | CA359697676 | FGF10 | c.530A>T (p.Tyr177Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.44305092T>C | CA359697677 | FGF10 | c.530A>G (p.Tyr177Cys) | |
| 5 | g.44305092T>G | CA359697678 | FGF10 | c.530A>C (p.Tyr177Ser) | |
| 5 | g.44305092T= | CA1543079586 | FGF10 | c.530A= (p.Tyr177=) | |
| 5 | g.44305093A>C | CA359697679 | FGF10 | c.529T>G (p.Tyr177Asp) | |
| 5 | g.44305093A>G | CA359697680 | FGF10 | c.529T>C (p.Tyr177His) | |
| 5 | g.44305093A>T | CA359697681 | FGF10 | c.529T>A (p.Tyr177Asn) | |
| 5 | g.44305094C>A | CA359697682 | FGF10 | c.528G>T (p.Met176Ile) | |
| 5 | g.44305094C>G | CA359697683 | FGF10 | c.528G>C (p.Met176Ile) | |
| 5 | g.44305094C>T | CA359697684 | FGF10 | c.528G>A (p.Met176Ile) | |
| 5 | g.44305095A>C | CA359697685 | FGF10 | c.527T>G (p.Met176Arg) | |
| 5 | g.44305095A>G | CA359697686 | FGF10 | c.527T>C (p.Met176Thr) | ClinVar |
| 5 | g.44305095A>T | CA359697687 | FGF10 | c.527T>A (p.Met176Lys) | gnomAD v3 gnomAD v4 |
| 5 | g.44305095_44305096delinsAT | CA1543079593 | FGF10 | c.526_527delinsAT (p.Met176=) | |
| 5 | g.44305096T>A | CA359697690 | FGF10 | c.526A>T (p.Met176Leu) | |
| 5 | g.44305096T>C | CA359697689 | FGF10 | c.526A>G (p.Met176Val) | |
| 5 | g.44305096T>G | CA359697688 | FGF10 | c.526A>C (p.Met176Leu) | |
| 5 | g.44305098del | CA658657443 | FGF10 | c.526del (p.Met176CysfsTer5) | ClinVar dbSNP |
| 5 | g.44305097T>A | CA359697691 | FGF10 | c.525A>T (p.Gln175His) | |
| 5 | g.44305097T>C | CA444230928 | FGF10 | c.525A>G (p.Gln175=) | gnomAD v4 |
| 5 | g.44305097T>G | CA359697692 | FGF10 | c.525A>C (p.Gln175His) | |
| 5 | g.44305098T>A | CA359697693 | FGF10 | c.524A>T (p.Gln175Leu) | |
| 5 | g.44305098T>C | CA359697694 | FGF10 | c.524A>G (p.Gln175Arg) | |
| 5 | g.44305098T>G | CA359697695 | FGF10 | c.524A>C (p.Gln175Pro) | |
| 5 | g.44305099G>A | CA359697696 | FGF10 | c.523C>T (p.Gln175Ter) | |
| 5 | g.44305099G>C | CA359697697 | FGF10 | c.523C>G (p.Gln175Glu) | |
| 5 | g.44305099G>T | CA359697698 | FGF10 | c.523C>A (p.Gln175Lys) | |
| 5 | g.44305100C>A | CA359697699 | FGF10 | c.522G>T (p.Arg174Ser) | |
| 5 | g.44305100C= | CA1543079608 | FGF10 | c.522G= (p.Arg174=) | |
| 5 | g.44305100C>G | CA359697700 | FGF10 | c.522G>C (p.Arg174Ser) | dbSNP |
| 5 | g.44305100C>T | CA444230929 | FGF10 | c.522G>A (p.Arg174=) | dbSNP gnomAD v4 COSMIC |
| 5 | g.44305101C>A | CA359697701 | FGF10 | c.521G>T (p.Arg174Met) | gnomAD v4 |
| 5 | g.44305101C= | CA1543079609 | FGF10 | c.521G= (p.Arg174=) | |
| 5 | g.44305101C>G | CA359697702 | FGF10 | c.521G>C (p.Arg174Thr) | dbSNP |
| 5 | g.44305101C>T | CA359697703 | FGF10 | c.521G>A (p.Arg174Lys) | dbSNP gnomAD v4 |
| 5 | g.44305102T>A | CA359697705 | FGF10 | c.520A>T (p.Arg174Trp) | |
| 5 | g.44305102T>C | CA359697704 | FGF10 | c.520A>G (p.Arg174Gly) | gnomAD v4 |
| 5 | g.44305102T>G | CA444230930 | FGF10 | c.520A>C (p.Arg174=) | |
| 5 | g.44305103C>A | CA444230931 | FGF10 | c.519G>T (p.Gly173=) | |
| 5 | g.44305103C>G | CA444230932 | FGF10 | c.519G>C (p.Gly173=) | |
| 5 | g.44305103C>T | CA444230933 | FGF10 | c.519G>A (p.Gly173=) | dbSNP |
| 5 | g.44305104C>A | CA359697706 | FGF10 | c.518G>T (p.Gly173Val) | |
| 5 | g.44305104C>G | CA359697708 | FGF10 | c.518G>C (p.Gly173Ala) | dbSNP |
| 5 | g.44305104C>T | CA359697707 | FGF10 | c.518G>A (p.Gly173Glu) | |
| 5 | g.44305105C>A | CA359697709 | FGF10 | c.517G>T (p.Gly173Trp) | dbSNP |
| 5 | g.44305105C= | CA1543079613 | FGF10 | c.517G= (p.Gly173=) | |
| 5 | g.44305105C>G | CA359697710 | FGF10 | c.517G>C (p.Gly173Arg) | dbSNP gnomAD v4 |
| 5 | g.44305105C>T | CA359697711 | FGF10 | c.517G>A (p.Gly173Arg) | gnomAD v4 |
| 5 | g.44305106A= | CA1543079619 | FGF10 | c.516T= (p.Asn172=) | |
| 5 | g.44305106A>C | CA359697712 | FGF10 | c.516T>G (p.Asn172Lys) | |
| 5 | g.44305106A>G | CA444230935 | FGF10 | c.516T>C (p.Asn172=) | dbSNP gnomAD v4 |
| 5 | g.44305106A>T | CA359697713 | FGF10 | c.516T>A (p.Asn172Lys) | |
| 5 | g.44305107T>A | CA359697714 | FGF10 | c.515A>T (p.Asn172Ile) | COSMIC |
| 5 | g.44305107T>C | CA359697715 | FGF10 | c.515A>G (p.Asn172Ser) | dbSNP |
| 5 | g.44305107T>G | CA359697716 | FGF10 | c.515A>C (p.Asn172Thr) | |
| 5 | g.44305107T= | CA1543079624 | FGF10 | c.515A= (p.Asn172=) | |
| 5 | g.44305108T>A | CA359697717 | FGF10 | c.514A>T (p.Asn172Tyr) | |
| 5 | g.44305108T>C | CA359697718 | FGF10 | c.514A>G (p.Asn172Asp) | gnomAD v4 |
| 5 | g.44305108T>G | CA359697719 | FGF10 | c.514A>C (p.Asn172His) | |
| 5 | g.44305109A>C | CA359697720 | FGF10 | c.513T>G (p.His171Gln) | |
| 5 | g.44305109A>G | CA444230936 | FGF10 | c.513T>C (p.His171=) | |
| 5 | g.44305109A>T | CA359697721 | FGF10 | c.513T>A (p.His171Gln) | |
| 5 | g.44305110T>A | CA359697724 | FGF10 | c.512A>T (p.His171Leu) | |
| 5 | g.44305110T>C | CA359697723 | FGF10 | c.512A>G (p.His171Arg) | |
| 5 | g.44305110T>G | CA359697722 | FGF10 | c.512A>C (p.His171Pro) | |
| 5 | g.44305111G>A | CA359697725 | FGF10 | c.511C>T (p.His171Tyr) | dbSNP |
| 5 | g.44305111G>C | CA359697726 | FGF10 | c.511C>G (p.His171Asp) | dbSNP |
| 5 | g.44305111G= | CA1543079630 | FGF10 | c.511C= (p.His171=) | |
| 5 | g.44305111G>T | CA359697727 | FGF10 | c.511C>A (p.His171Asn) | dbSNP gnomAD v4 |
| 5 | g.44305112C>A | CA359697728 | FGF10 | c.510G>T (p.Gln170His) | |
| 5 | g.44305112C= | CA1543079636 | FGF10 | c.510G= (p.Gln170=) | |
| 5 | g.44305112C>G | CA359697729 | FGF10 | c.510G>C (p.Gln170His) | |
| 5 | g.44305112C>T | CA118160550 | FGF10 | c.510G>A (p.Gln170=) | dbSNP gnomAD v4 |
| 5 | g.44305113T>A | CA359697730 | FGF10 | c.509A>T (p.Gln170Leu) | |
| 5 | g.44305113T>C | CA359697731 | FGF10 | c.509A>G (p.Gln170Arg) | gnomAD v4 |
| 5 | g.44305113T>G | CA359697732 | FGF10 | c.509A>C (p.Gln170Pro) | |
| 5 | g.44305114G>A | CA359697733 | FGF10 | c.508C>T (p.Gln170Ter) | dbSNP |
| 5 | g.44305114G>C | CA359697734 | FGF10 | c.508C>G (p.Gln170Glu) | |
| 5 | g.44305114G= | CA1543079638 | FGF10 | c.508C= (p.Gln170=) | |
| 5 | g.44305114G>T | CA3258484 | FGF10 | c.508C>A (p.Gln170Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.44305115C>A | CA359697735 | FGF10 | c.507G>T (p.Trp169Cys) | |
| 5 | g.44305115C>G | CA359697736 | FGF10 | c.507G>C (p.Trp169Cys) | |
| 5 | g.44305115C>T | CA359697737 | FGF10 | c.507G>A (p.Trp169Ter) | dbSNP |
| 5 | g.44305116C>A | CA359697739 | FGF10 | c.506G>T (p.Trp169Leu) | |
| 5 | g.44305116C>G | CA359697740 | FGF10 | c.506G>C (p.Trp169Ser) | |
| 5 | g.44305116C>T | CA359697738 | FGF10 | c.506G>A (p.Trp169Ter) | dbSNP |
| 5 | g.44305117A>C | CA359697741 | FGF10 | c.505T>G (p.Trp169Gly) | |
| 5 | g.44305117A>G | CA359697742 | FGF10 | c.505T>C (p.Trp169Arg) | |
| 5 | g.44305117A>T | CA359697743 | FGF10 | c.505T>A (p.Trp169Arg) | |
| 5 | g.44305118G>A | CA118160551 | FGF10 | c.504C>T (p.Asn168=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.44305118G>C | CA359697744 | FGF10 | c.504C>G (p.Asn168Lys) | |
| 5 | g.44305118G= | CA1543079646 | FGF10 | c.504C= (p.Asn168=) | |
| 5 | g.44305118G>T | CA359697745 | FGF10 | c.504C>A (p.Asn168Lys) | dbSNP |
| 5 | g.44305119T>A | CA359697746 | FGF10 | c.503A>T (p.Asn168Ile) | |
| 5 | g.44305119T>C | CA359697747 | FGF10 | c.503A>G (p.Asn168Ser) | |
| 5 | g.44305119T>G | CA359697748 | FGF10 | c.503A>C (p.Asn168Thr) | |
| 5 | g.44305120T>A | CA359697749 | FGF10 | c.502A>T (p.Asn168Tyr) | |
| 5 | g.44305120T>C | CA359697750 | FGF10 | c.502A>G (p.Asn168Asp) | gnomAD v4 |
| 5 | g.44305120T>G | CA359697751 | FGF10 | c.502A>C (p.Asn168His) | |
| 5 | g.44305121A>C | CA359697752 | FGF10 | c.501T>G (p.Phe167Leu) | |
| 5 | g.44305121A>G | CA444230940 | FGF10 | c.501T>C (p.Phe167=) | |
| 5 | g.44305121A>T | CA359697753 | FGF10 | c.501T>A (p.Phe167Leu) | |
| 5 | g.44305122A>C | CA359697754 | FGF10 | c.500T>G (p.Phe167Cys) | |
| 5 | g.44305122A>G | CA359697756 | FGF10 | c.500T>C (p.Phe167Ser) | |
| 5 | g.44305122A>T | CA359697755 | FGF10 | c.500T>A (p.Phe167Tyr) | |
| 5 | g.44305123A= | CA1543079649 | FGF10 | c.499T= (p.Phe167=) | |
| 5 | g.44305123A>C | CA359697757 | FGF10 | c.499T>G (p.Phe167Val) | |
| 5 | g.44305123A>G | CA359697758 | FGF10 | c.499T>C (p.Phe167Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.44305123A>T | CA359697759 | FGF10 | c.499T>A (p.Phe167Ile) | |
| 5 | g.44305124T>A | CA444230941 | FGF10 | c.498A>T (p.Ser166=) | |
| 5 | g.44305124T>C | CA3258485 | FGF10 | c.498A>G (p.Ser166=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.44305124T>G | CA444230942 | FGF10 | c.498A>C (p.Ser166=) | |
| 5 | g.44305124T= | CA1543079654 | FGF10 | c.498A= (p.Ser166=) | |
| 5 | g.44305125G>A | CA359697760 | FGF10 | c.497C>T (p.Ser166Leu) | |
| 5 | g.44305125G>C | CA359697761 | FGF10 | c.497C>G (p.Ser166Ter) | |
| 5 | g.44305125G>T | CA359697762 | FGF10 | c.497C>A (p.Ser166Ter) | |
| 5 | g.44305126A>C | CA359697763 | FGF10 | c.496T>G (p.Ser166Ala) | |
| 5 | g.44305126A>G | CA359697764 | FGF10 | c.496T>C (p.Ser166Pro) | gnomAD v4 |
| 5 | g.44305126A>T | CA359697765 | FGF10 | c.496T>A (p.Ser166Thr) | |
| 5 | g.44305127T>A | CA444230943 | FGF10 | c.495A>T (p.Ala165=) | |
| 5 | g.44305127T>C | CA444230944 | FGF10 | c.495A>G (p.Ala165=) | gnomAD v4 |
| 5 | g.44305127T>G | CA444230945 | FGF10 | c.495A>C (p.Ala165=) | |
| 5 | g.44305128G>A | CA359697768 | FGF10 | c.494C>T (p.Ala165Val) | dbSNP |
| 5 | g.44305128G>C | CA359697767 | FGF10 | c.494C>G (p.Ala165Gly) | |
| 5 | g.44305128G>T | CA359697766 | FGF10 | c.494C>A (p.Ala165Glu) | |
| 5 | g.44305129C>A | CA359697769 | FGF10 | c.493G>T (p.Ala165Ser) | dbSNP |
| 5 | g.44305129C>G | CA359697771 | FGF10 | c.493G>C (p.Ala165Pro) | |
| 5 | g.44305129C>T | CA359697770 | FGF10 | c.493G>A (p.Ala165Thr) | |
| 5 | g.44305130A= | CA1543079677 | FGF10 | c.492T= (p.Tyr164=) | |
| 5 | g.44305130A>C | CA359697772 | FGF10 | c.492T>G (p.Tyr164Ter) | |
| 5 | g.44305130A>G | CA3258486 | FGF10 | c.492T>C (p.Tyr164=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.44305130A>T | CA359697773 | FGF10 | c.492T>A (p.Tyr164Ter) | |
| 5 | g.44305131T>A | CA359697774 | FGF10 | c.491A>T (p.Tyr164Phe) | |
| 5 | g.44305131T>C | CA359697775 | FGF10 | c.491A>G (p.Tyr164Cys) | |
| 5 | g.44305131T>G | CA359697776 | FGF10 | c.491A>C (p.Tyr164Ser) | |
| 5 | g.44305132A>C | CA359697777 | FGF10 | c.490T>G (p.Tyr164Asp) | |
| 5 | g.44305132A>G | CA359697778 | FGF10 | c.490T>C (p.Tyr164His) | |
| 5 | g.44305132A>T | CA359697779 | FGF10 | c.490T>A (p.Tyr164Asn) | |
| 5 | g.44305133G>A | CA444230946 | FGF10 | c.489C>T (p.Thr163=) | dbSNP |
| 5 | g.44305133G>C | CA444230947 | FGF10 | c.489C>G (p.Thr163=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.44305133G= | CA1543079678 | FGF10 | c.489C= (p.Thr163=) | |
| 5 | g.44305133G>T | CA3258487 | FGF10 | c.489C>A (p.Thr163=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.44305134G>A | CA359697780 | FGF10 | c.488C>T (p.Thr163Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.44305134G>C | CA359697781 | FGF10 | c.488C>G (p.Thr163Ser) | |
| 5 | g.44305134G= | CA1543079679 | FGF10 | c.488C= (p.Thr163=) | |
| 5 | g.44305134G>T | CA359697782 | FGF10 | c.488C>A (p.Thr163Asn) | |
| 5 | g.44305135T>A | CA359697783 | FGF10 | c.487A>T (p.Thr163Ser) | |
| 5 | g.44305135T>C | CA359697785 | FGF10 | c.487A>G (p.Thr163Ala) | |
| 5 | g.44305135T>G | CA359697784 | FGF10 | c.487A>C (p.Thr163Pro) | |
| 5 | g.44305136A>C | CA359697786 | FGF10 | c.486T>G (p.Asn162Lys) | |
| 5 | g.44305136A>G | CA444230948 | FGF10 | c.486T>C (p.Asn162=) | COSMIC |
| 5 | g.44305136A>T | CA359697787 | FGF10 | c.486T>A (p.Asn162Lys) | |
| 5 | g.44305137T>A | CA359697788 | FGF10 | c.485A>T (p.Asn162Ile) | |
| 5 | g.44305137T>C | CA359697789 | FGF10 | c.485A>G (p.Asn162Ser) | |
| 5 | g.44305137T>G | CA359697790 | FGF10 | c.485A>C (p.Asn162Thr) | |
| 5 | g.44305138T>A | CA359697791 | FGF10 | c.484A>T (p.Asn162Tyr) | |
| 5 | g.44305138T>C | CA359697792 | FGF10 | c.484A>G (p.Asn162Asp) | gnomAD v4 |
| 5 | g.44305138T>G | CA359697793 | FGF10 | c.484A>C (p.Asn162His) | |
| 5 | g.44305139G>A | CA444230950 | FGF10 | c.483C>T (p.Tyr161=) | dbSNP gnomAD v4 |
| 5 | g.44305139G>C | CA359697794 | FGF10 | c.483C>G (p.Tyr161Ter) | |
| 5 | g.44305139G= | CA1543079680 | FGF10 | c.483C= (p.Tyr161=) | |
| 5 | g.44305139G>T | CA359697795 | FGF10 | c.483C>A (p.Tyr161Ter) | |
| 5 | g.44305140T>A | CA359697798 | FGF10 | c.482A>T (p.Tyr161Phe) | gnomAD v4 |
| 5 | g.44305140T>C | CA359697797 | FGF10 | c.482A>G (p.Tyr161Cys) | gnomAD v4 |
| 5 | g.44305140T>G | CA359697796 | FGF10 | c.482A>C (p.Tyr161Ser) | |
| 5 | g.44305141A>C | CA359697799 | FGF10 | c.481T>G (p.Tyr161Asp) | dbSNP |
| 5 | g.44305141A>G | CA359697800 | FGF10 | c.481T>C (p.Tyr161His) | |
| 5 | g.44305141A>T | CA359697801 | FGF10 | c.481T>A (p.Tyr161Asn) | |
| 5 | g.44305142T>A | CA444230951 | FGF10 | c.480A>T (p.Gly160=) | gnomAD v4 |
| 5 | g.44305142T>C | CA444230952 | FGF10 | c.480A>G (p.Gly160=) | gnomAD v4 |
| 5 | g.44305142T>G | CA444230953 | FGF10 | c.480A>C (p.Gly160=) | |
| 5 | g.44305143C>A | CA359697802 | FGF10 | c.479G>T (p.Gly160Val) | |
| 5 | g.44305143C>G | CA359697803 | FGF10 | c.479G>C (p.Gly160Ala) | |
| 5 | g.44305143C>T | CA359697804 | FGF10 | c.479G>A (p.Gly160Glu) | dbSNP |
| 5 | g.44305144C>A | CA359697805 | FGF10 | c.478G>T (p.Gly160Ter) | |
| 5 | g.44305144C>G | CA359697806 | FGF10 | c.478G>C (p.Gly160Arg) | |
| 5 | g.44305144C>T | CA359697807 | FGF10 | c.478G>A (p.Gly160Arg) | |
| 5 | g.44305145A= | CA1543079681 | FGF10 | c.477T= (p.Asn159=) | |
| 5 | g.44305145A>C | CA359697808 | FGF10 | c.477T>G (p.Asn159Lys) | |
| 5 | g.44305145A>G | CA118160552 | FGF10 | c.477T>C (p.Asn159=) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.44305145A>T | CA359697809 | FGF10 | c.477T>A (p.Asn159Lys) | COSMIC |
| 5 | g.44305146T>A | CA359697811 | FGF10 | c.476A>T (p.Asn159Ile) | |
| 5 | g.44305146T>C | CA359697812 | FGF10 | c.476A>G (p.Asn159Ser) | |
| 5 | g.44305146T>G | CA359697810 | FGF10 | c.476A>C (p.Asn159Thr) | |
| 5 | g.44305149dup | CA2578304748 | FGF10 | c.476dup (p.Asn159LysfsTer10) | |
| 5 | g.44305149del | CA2708817195 | FGF10 | c.476del (p.Asn159MetfsTer22) | dbSNP |
| 5 | g.44305147T>A | CA359697813 | FGF10 | c.475A>T (p.Asn159Tyr) | |
| 5 | g.44305147T>C | CA359697814 | FGF10 | c.475A>G (p.Asn159Asp) | |
| 5 | g.44305147T>G | CA359697815 | FGF10 | c.475A>C (p.Asn159His) | gnomAD v4 |
| 5 | g.44305148T>A | CA359697816 | FGF10 | c.474A>T (p.Glu158Asp) | |
| 5 | g.44305148T>C | CA118160553 | FGF10 | c.474A>G (p.Glu158=) | dbSNP |
| 5 | g.44305148T>G | CA359697817 | FGF10 | c.474A>C (p.Glu158Asp) | |
| 5 | g.44305148T= | CA1543079682 | FGF10 | c.474A= (p.Glu158=) | |
| 5 | g.44305149T>A | CA359697820 | FGF10 | c.473A>T (p.Glu158Val) | |
| 5 | g.44305149T>C | CA359697818 | FGF10 | c.473A>G (p.Glu158Gly) | dbSNP |
| 5 | g.44305149T>G | CA359697819 | FGF10 | c.473A>C (p.Glu158Ala) | |
| 5 | g.44305150C>A | CA359697821 | FGF10 | c.472G>T (p.Glu158Ter) | |
| 5 | g.44305150C>G | CA359697822 | FGF10 | c.472G>C (p.Glu158Gln) | |
| 5 | g.44305150C>T | CA359697823 | FGF10 | c.472G>A (p.Glu158Lys) | dbSNP gnomAD v4 COSMIC |
| 5 | g.44305151C>A | CA359697824 | FGF10 | c.471G>T (p.Glu157Asp) | dbSNP COSMIC |
| 5 | g.44305151C>G | CA359697825 | FGF10 | c.471G>C (p.Glu157Asp) | |
| 5 | g.44305151C>T | CA444230955 | FGF10 | c.471G>A (p.Glu157=) | dbSNP gnomAD v4 |
| 5 | g.44305152T>A | CA359697828 | FGF10 | c.470A>T (p.Glu157Val) | |
| 5 | g.44305152T>C | CA359697827 | FGF10 | c.470A>G (p.Glu157Gly) | |
| 5 | g.44305152T>G | CA359697826 | FGF10 | c.470A>C (p.Glu157Ala) | |
| 5 | g.44305153C>A | CA359697829 | FGF10 | c.469G>T (p.Glu157Ter) | |
| 5 | g.44305153C>G | CA359697831 | FGF10 | c.469G>C (p.Glu157Gln) | gnomAD v4 |
| 5 | g.44305153C>T | CA359697830 | FGF10 | c.469G>A (p.Glu157Lys) | COSMIC |
| 5 | g.44305154T>A | CA444230956 | FGF10 | c.468A>T (p.Ile156=) | |
| 5 | g.44305154T>C | CA359697832 | FGF10 | c.468A>G (p.Ile156Met) | |
| 5 | g.44305154T>G | CA444230957 | FGF10 | c.468A>C (p.Ile156=) | |
| 5 | g.44305155A= | CA1543079689 | FGF10 | c.467T= (p.Ile156=) | |
| 5 | g.44305155A>C | CA118869 | FGF10 | c.467T>G (p.Ile156Arg) | ClinVar dbSNP |
| 5 | g.44305155A>G | CA359697833 | FGF10 | c.467T>C (p.Ile156Thr) | |
| 5 | g.44305155A>T | CA359697834 | FGF10 | c.467T>A (p.Ile156Lys) | |
| 5 | g.44305156T>A | CA359697835 | FGF10 | c.466A>T (p.Ile156Leu) | |
| 5 | g.44305156T>C | CA359697837 | FGF10 | c.466A>G (p.Ile156Val) | |
| 5 | g.44305156T>G | CA359697836 | FGF10 | c.466A>C (p.Ile156Leu) | |
| 5 | g.44305157C>A | CA359697838 | FGF10 | c.465G>T (p.Arg155Ser) | |
| 5 | g.44305157C= | CA1543079693 | FGF10 | c.465G= (p.Arg155=) | |
| 5 | g.44305157C>G | CA359697839 | FGF10 | c.465G>C (p.Arg155Ser) | |
| 5 | g.44305157C>T | CA3258488 | FGF10 | c.465G>A (p.Arg155=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.44305158C>A | CA359697840 | FGF10 | c.464G>T (p.Arg155Met) | dbSNP |
| 5 | g.44305158C= | CA1543079698 | FGF10 | c.464G= (p.Arg155=) | |
| 5 | g.44305158C>G | CA359697842 | FGF10 | c.464G>C (p.Arg155Thr) | |
| 5 | g.44305158C>T | CA359697841 | FGF10 | c.464G>A (p.Arg155Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.44305159T>A | CA359697843 | FGF10 | c.463A>T (p.Arg155Trp) | |
| 5 | g.44305159T>C | CA359697844 | FGF10 | c.463A>G (p.Arg155Gly) | |
| 5 | g.44305159T>G | CA444230960 | FGF10 | c.463A>C (p.Arg155=) | |
| 5 | g.44305160C>A | CA359697845 | FGF10 | c.462G>T (p.Glu154Asp) | |
| 5 | g.44305160C= | CA1543079701 | FGF10 | c.462G= (p.Glu154=) | |
| 5 | g.44305160C>G | CA359697846 | FGF10 | c.462G>C (p.Glu154Asp) | |
| 5 | g.44305160C>T | CA444230961 | FGF10 | c.462G>A (p.Glu154=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.44305161T>A | CA359697847 | FGF10 | c.461A>T (p.Glu154Val) | |
| 5 | g.44305161T>C | CA359697848 | FGF10 | c.461A>G (p.Glu154Gly) | |
| 5 | g.44305161T>G | CA359697849 | FGF10 | c.461A>C (p.Glu154Ala) | |
| 5 | g.44305162C>A | CA359697850 | FGF10 | c.460G>T (p.Glu154Ter) | |
| 5 | g.44305162C>G | CA359697851 | FGF10 | c.460G>C (p.Glu154Gln) | |
| 5 | g.44305162C>T | CA359697852 | FGF10 | c.460G>A (p.Glu154Lys) | |
| 5 | g.44305163C>A | CA359697854 | FGF10 | c.459G>T (p.Lys153Asn) | |
| 5 | g.44305163C>G | CA359697853 | FGF10 | c.459G>C (p.Lys153Asn) | |
| 5 | g.44305163C>T | CA444230962 | FGF10 | c.459G>A (p.Lys153=) | |
| 5 | g.44305164T>A | CA359697855 | FGF10 | c.458A>T (p.Lys153Met) | |
| 5 | g.44305164T>C | CA359697856 | FGF10 | c.458A>G (p.Lys153Arg) | |
| 5 | g.44305164T>G | CA359697857 | FGF10 | c.458A>C (p.Lys153Thr) | |
| 5 | g.44305165T>A | CA359697858 | FGF10 | c.457A>T (p.Lys153Ter) | |
| 5 | g.44305165T>C | CA359697859 | FGF10 | c.457A>G (p.Lys153Glu) | |
| 5 | g.44305165T>G | CA359697860 | FGF10 | c.457A>C (p.Lys153Gln) |