Product Details

SNP ID

rs11231342

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63081096 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGTGCTGCCCCAGTCCTACCGGA[C/G]ACTGCATTGATTCCTGCAACTGTTG

Phenotype

MIM: 611698

Polymorphism

C/G, Transversion 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	1864	Silent Mutation	GTC,GTG	V474V	NP_001129978.2
NM_173586.2	1864	Intron			NP_775857.2
XM_011544967.2	1864	Intron			XP_011543269.1

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