Product Details

SNP ID

rs121912683

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:185145020 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTAACCTGGCGTCCGGTGGGGCCG[A/C]TGGGGCCACCTCCCTTTGCTTTGTC

Phenotype

MIM: 103220

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC25A4 PubMed Links

Gene Details

Gene

SLC25A4

Gene Name

solute carrier family 25 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001151.3	478	Missense Mutation	GAT,GCT	D123A	NP_001142.2

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