Product Details

SNP ID
rs150845678
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:38846977 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATTGCTTTCATACTATCTAGGCCA[G/T]CAGAGCCACCGAGTACCCTAGCGGT
Phenotype
MIM: 604385
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SCN11A PubMed Links

Gene Details

Gene
SCN11A
Gene Name
sodium voltage-gated channel alpha subunit 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287223.1 3901 Missense Mutation GAT,GCT D1698A NP_001274152.1
NM_014139.2 3901 Missense Mutation GAT,GCT D1698A NP_054858.2
XM_011533321.2 3901 Missense Mutation GAT,GCT D1477A XP_011531623.1
XM_017005647.1 3901 Missense Mutation GAT,GCT D1823A XP_016861136.1
XM_017005648.1 3901 Missense Mutation GAT,GCT D1632A XP_016861137.1
XM_017005649.1 3901 Missense Mutation GAT,GCT D1698A XP_016861138.1
XM_017005650.1 3901 Missense Mutation GAT,GCT D1698A XP_016861139.1
XM_017005651.1 3901 Missense Mutation GAT,GCT D1607A XP_016861140.1
XM_017005652.1 3901 Intron XP_016861141.1
XM_017005653.1 3901 Missense Mutation GAT,GCT D1166A XP_016861142.1

View Full Product Details