No paralogue variants have been mapped to residue 873 for SCN5A.
SCN5A | IVFIFAVVGMQLFGKNYSEL-RDS----D->S<G---LLPRWHMMDFFHAFLIIFRILCGE-W | 899 |
SCN1A | IVFIFAVVGMQLFGKSYKDC-VCK----I->A<S-DCQLPRWHMNDFFHSFLIVFRVLCGE-W | 952 |
SCN2A | IVFIFAVVGMQLFGKSYKEC-VCK----I->S<N-DCELPRWHMHDFFHSFLIVFRVLCGE-W | 943 |
SCN3A | IVFIFAVVGMQLFGKSYKEC-VCK----I->N<D-DCTLPRWHMNDFFHSFLIVFRVLCGE-W | 944 |
SCN4A | IVFIFAVVGMQLFGKSYKEC-VCK----I->A<L-DCNLPRWHMHDFFHSFLIVFRILCGE-W | 762 |
SCN7A | FIFFSAAFGMKLFGKNYEEF-VCH----I->D<K-DCQLPRWHMHDFFHSFLNVFRILCGE-W | 689 |
SCN8A | IVFIFAVVGMQLFGKSYKEC-VCK----I->N<Q-DCELPRWHMHDFFHSFLIVFRVLCGE-W | 937 |
SCN9A | IVFIFAVVGMQLFGKSYKEC-VCK----I->N<D-DCTLPRWHMNDFFHSFLIVFRVLCGE-W | 917 |
SCN10A | IVFVFALVGKQLLGENYRNN-RKN----I->S<APHEDWPRWHMHDFFHSFLIVFRILCGE-W | 850 |
SCN11A | VIFIFSVVGMQLFGRSFNSQ-KSPKLCNPT>G<PTVSCLRHWHMGDFWHSFLVVFRILCGE-W | 769 |
CACNA1A | FIVVFALLGMQLFGGQFNFD-E-------->-<---G-TPPTNFDTFPAAIMTVFQILTGEDW | 670 |
CACNA1B | FIVVFALLGMQLFGGQFNFQ-D-------->-<---E-TPTTNFDTFPAAILTVFQILTGEDW | 666 |
CACNA1C | FIIIFSLLGMQLFGGKFNFD-E-------->-<---MQTRRSTFDNFPQSLLTVFQILTGEDW | 708 |
CACNA1D | FIIIFSLLGMQLFGGKFNFD-E-------->-<---TQTKRSTFDNFPQALLTVFQILTGEDW | 727 |
CACNA1E | FIVVFALLGMQLFGGRFNFN-D-------->-<---G-TPSANFDTFPAAIMTVFQILTGEDW | 659 |
CACNA1F | FIIIFSLLGMQLFGGKFNFD-Q-------->-<---THTKRSTFDTFPQALLTVFQILTGEDW | 713 |
CACNA1G | FIFIFSILGMHLFGCKFASER--------->D<G-DTLPDRKNFDSLLWAIVTVFQILTQEDW | 925 |
CACNA1H | FIFIFSILGMHLFGCKFSLKTD-------->T<G-DTVPDRKNFDSLLWAIVTVFQILTQEDW | 976 |
CACNA1I | FIFIFSILGMHIFGCKFSLRTD-------->T<G-DTVPDRKNFDSLLWAIVTVFQILTQEDW | 823 |
CACNA1S | FIVIFALLGMQLFGGRYDFE-D-------->-<---TEVRRSNFDNFPQALISVFQVLTGEDW | 616 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.S873A | c.2617T>G | Putative Benign | SIFT: Polyphen: | ||
p.Ser873Leu | c.2618C>T | Unknown | SIFT: Polyphen: |