Paralogue Annotation for SCN5A residue 751

Residue details

Gene: SCN5A
Reference Sequences: LRG: LRG_289, Ensembl variant: ENST00000333535 / ENSP00000328968
Amino Acid Position: 751
Reference Amino Acid: V - Valine
Protein Domain: TM Domain 2


Paralogue Variants mapped to SCN5A residue 751

No paralogue variants have been mapped to residue 751 for SCN5A.



SCN5ALTITMCIVLNTLFMALEHYNMTSEFEEMLQ>V<GNLVFTGIFTAEMTFKIIALDPYYYFQQGW781
SCN1ALAITICIVLNTLFMAMEHYPMTDHFNNVLT>V<GNLVFTGIFTAEMFLKIIAMDPYYYFQEGW832
SCN2ALAITICIVLNTLFMAMEHYPMTEQFSSVLS>V<GNLVFTGIFTAEMFLKIIAMDPYYYFQEGW823
SCN3ALAITICIVLNTLFMAMEHYPMTEQFSSVLT>V<GNLVFTGIFTAEMVLKIIAMDPYYYFQEGW824
SCN4ALGITICIVLNTLFMAMEHYPMTEHFDNVLT>V<GNLVFTGIFTAEMVLKLIAMDPYEYFQQGW642
SCN7ALFLIICIILNVCFLTLEHYPMSKQTNTLLN>I<GNLVFIGIFTAEMIFKIIAMHPYGYFQVGW569
SCN8ALAITICIVLNTLFMAMEHHPMTPQFEHVLA>V<GNLVFTGIFTAEMFLKLIAMDPYYYFQEGW817
SCN9ALAITICIVLNTLFMAMEHHPMTEEFKNVLA>I<GNLVFTGIFAAEMVLKLIAMDPYEYFQVGW797
SCN10ALTITLCIVVNTIFMAMEHHGMSPTFEAMLQ>I<GNIVFTIFFTAEMVFKIIAFDPYYYFQKKW729
SCN11ALAITICIIINTVFLAMEHHKMEASFEKMLN>I<GNLVFTSIFIAEMCLKIIALDPYHYFRRGW641
CACNA1AWTVLSLVALNTLCVAIVHYNQPEWLSDFLY>Y<AEFIFLGLFMSEMFIKMYGLGTRPYFHSSF551
CACNA1BWVVLCVVALNTLCVAMVHYNQPRRLTTTLY>F<AEFVFLGLFLTEMSLKMYGLGPRSYFRSSF547
CACNA1CWLVIFLVFLNTLTIASEHYNQPNWLTEVQD>T<ANKALLALFTAEMLLKMYSLGLQAYFVSLF588
CACNA1DWLVIVLVFLNTLTISSEHYNQPDWLTQIQD>I<ANKVLLALFTCEMLVKMYSLGLQAYFVSLF607
CACNA1EWIVLSLVALNTACVAIVHHNQPQWLTHLLY>Y<AEFLFLGLFLLEMSLKMYGMGPRLYFHSSF540
CACNA1FWAVLLLVFLNTLTIASEHHGQPVWLTQIQE>Y<ANKVLLCLFTVEMLLKLYGLGPSAYVSSFF593
CACNA1GRGIMIAILVNTLSMGIEYHEQPEELTNALE>I<SNIVFTSLFALEMLLKLLVYGPFGYIKNPY807
CACNA1HRGIMMAILVNTLSMGVEYHEQPEELTNALE>I<SNIVFTSMFALEMLLKLLACGPLGYIRNPY857
CACNA1IRGIMMAILVNTVSMGIEHHEQPEELTNILE>I<CNVVFTSMFALEMILKLAAFGLFDYLRNPY704
CACNA1SWLVILIVALNTLSIASEHHNQPLWLTRLQD>I<ANRVLLSLFTTEMLMKMYGLGLRQYFMSIF496
cons                              > <                              

See full Alignment of Paralogues


Known Variants in SCN5A

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.V751Ic.2251G>A Putative BenignSIFT:
Polyphen:
p.V751Fc.2251G>T Putative BenignSIFT:
Polyphen: