Product Details

SNP ID

rs144530892

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103400533 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGCAATTCCCTTGTAAAATCCAC[C/T]GACGCCTTCTTTCCTTTAGAGGGAA

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	1224	Missense Mutation	AGT,GGT	S276G	NP_110407.2
XM_017013877.1	1224	Missense Mutation	AGT,GGT	S144G	XP_016869366.1

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