Product Details

SNP ID

rs141367018

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103401586 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTGATCCTGAAGACGAGCTCTTA[C/T]GACTTGATATGGGTATGTTGCTGCG

Phenotype

MIM: 610815

Polymorphism

C/T, Transition 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	1140	Missense Mutation	ATA,GTA	I248V	NP_110407.2
XM_017013877.1	1140	Missense Mutation	ATA,GTA	I116V	XP_016869366.1

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