Product Details

SNP ID
rs142887458
Assay Type
Functionally Tested
NCBI dbSNP Submissions
3
Location
Chr.1:27100626 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGATGACAGGCAGGTCCTCCTTC[A/G]GCTCATAGGCCAGTGGGTCTGGGGA
Phenotype
MIM: 107310
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC9A1 PubMed Links

Gene Details

Gene
SLC9A1
Gene Name
solute carrier family 9 member A1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003047.4 2003 Missense Mutation CCG,CTG P710L NP_003038.2
XM_011542021.2 2003 Missense Mutation CCG,CTG P600L XP_011540323.1

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