Product Details

SNP ID

rs145785157

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103401630 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGCGACAGCAAATATTTTGGAT[A/G]GTGCTGCAACAGATATATATTCTAC

Phenotype

MIM: 610815

Polymorphism

A/G, 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	1096	Missense Mutation	CCA,CTA	P233L	NP_110407.2
XM_017013877.1	1096	Missense Mutation	CCA,CTA	P101L	XP_016869366.1

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