Product Details

SNP ID

rs7945121

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63079981 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCATGCAAGTATCTTCCTGCTTTA[C/T]GTTTCTTGAATCTTTTCTGCTGAGA

Phenotype

MIM: 611698

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC22A24 PubMed Links

Gene Details

Gene

SLC22A24

Gene Name

solute carrier family 22 member 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136506.2	2060	Missense Mutation	ATA,GTA	I540V	NP_001129978.2
NM_173586.2	2060	Intron			NP_775857.2
XM_011544967.2	2060	Intron			XP_011543269.1

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