Product Details

SNP ID
rs145589241
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:38697971 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAACTGAGTGGCCTCTGGGTCAAAC[C/T]TCTCCCAGGTCTCATAGAACATGTC
Phenotype
MIM: 604427
Polymorphism
C/T, Transition 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 4955 Missense Mutation AAG,AGG K1749R NP_001280235.2
NM_001293307.2 4955 Missense Mutation AAG,AGG K1652R NP_001280236.2
NM_006514.3 4955 Missense Mutation AAG,AGG K1750R NP_006505.3
XM_005265371.3 4955 Missense Mutation AAG,AGG K1753R XP_005265428.1
XM_011533993.2 4955 Missense Mutation AAG,AGG K1752R XP_011532295.1
XM_011533994.2 4955 Missense Mutation AAG,AGG K1655R XP_011532296.1

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