Product Details

SNP ID

rs148952091

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103401985 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTATTGATATGCTGGTTGTACTTCA[A/T]CTTCAGCAATTCATATGCCATAAAC

Phenotype

MIM: 610815

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC25A32 PubMed Links

Gene Details

Gene

SLC25A32

Gene Name

solute carrier family 25 member 32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030780.4	1020	Missense Mutation	ATG,TTG	M208L	NP_110407.2
XM_017013877.1	1020	Missense Mutation	ATG,TTG	M76L	XP_016869366.1

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