Product Details

SNP ID

rs200765659

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:65624274 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCAGCCTATAAAACTGGCCAGTC[G/T]GGACCTCTCCAGTGAAGAGATGATG

Phenotype

MIM: 603617

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC24A1 PubMed Links

Gene Details

Gene

SLC24A1

Gene Name

solute carrier family 24 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001254740.1	455	Intron			NP_001241669.1
NM_001301031.1	455	Missense Mutation	CGG,CTG	R65L	NP_001287960.1
NM_001301032.1	455	Missense Mutation	CGG,CTG	R65L	NP_001287961.1
NM_001301033.1	455	Missense Mutation	CGG,CTG	R65L	NP_001287962.1
NM_004727.2	455	Missense Mutation	CGG,CTG	R65L	NP_004718.1
XM_005254778.3	455	Missense Mutation	CGG,CTG	R65L	XP_005254835.1
XM_005254781.3	455	Missense Mutation	CGG,CTG	R65L	XP_005254838.1
XM_006720768.3	455	Missense Mutation	CGG,CTG	R65L	XP_006720831.1
XM_011522219.1	455	Missense Mutation	CGG,CTG	R65L	XP_011520521.1
XM_011522220.2	455	Missense Mutation	CGG,CTG	R65L	XP_011520522.1
XM_011522221.2	455	Missense Mutation	CGG,CTG	R65L	XP_011520523.1
XM_011522222.2	455	Missense Mutation	CGG,CTG	R65L	XP_011520524.1
XM_011522226.2	455	Missense Mutation	CGG,CTG	R65L	XP_011520528.1
XM_017022724.1	455	Missense Mutation	CGG,CTG	R65L	XP_016878213.1
XM_017022725.1	455	Missense Mutation	CGG,CTG	R65L	XP_016878214.1

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