Product Details

SNP ID

rs199841831

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:48121148 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTCAGGGACCTCCCTGCCCCAAC[A/G]TCTCCCAAGGGCCACAGGTAGGTGG

Phenotype

MIM: 609802

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC24A5 PubMed Links

Gene Details

Gene

SLC24A5

Gene Name

solute carrier family 24 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_205850.2	177	Missense Mutation	CAT,CGT	H35R	NP_995322.1
XM_017022079.1	177	Intron			XP_016877568.1
XM_017022080.1	177	Intron			XP_016877569.1

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