Product Details

SNP ID

rs140566252

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:38697850 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATCTTATCTCCAGGGACCAAAGG[A/C]AGGTCCATCTGGATCAGTATATTTC

Phenotype

MIM: 604427

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SCN10A PubMed Links

Gene Details

Gene

SCN10A

Gene Name

sodium voltage-gated channel alpha subunit 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001293306.2	5076	Silent Mutation	CTG,CTT	L1789L	NP_001280235.2
NM_001293307.2	5076	Silent Mutation	CTG,CTT	L1692L	NP_001280236.2
NM_006514.3	5076	Silent Mutation	CTG,CTT	L1790L	NP_006505.3
XM_005265371.3	5076	Silent Mutation	CTG,CTT	L1793L	XP_005265428.1
XM_011533993.2	5076	Silent Mutation	CTG,CTT	L1792L	XP_011532295.1
XM_011533994.2	5076	Silent Mutation	CTG,CTT	L1695L	XP_011532296.1

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