Product Details

SNP ID

rs7854499

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128085662 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTTTTCTGATCTCTTAGGGTGGAA[A/G]CTGAAGTCACTGATTTTGAGACCTT

Phenotype

MIM: 608745

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC25A25 PubMed Links

Gene Details

Gene

SLC25A25

Gene Name

solute carrier family 25 member 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001006641.3		Intron			NP_001006642.1
NM_001006642.3		Intron			NP_001006643.1
NM_001265614.2		Intron			NP_001252543.1
NM_052901.4		Intron			NP_443133.2
XM_005251688.1		Intron			XP_005251745.1
XM_005251689.4		Intron			XP_005251746.1
XM_006716948.2		Intron			XP_006717011.1
XM_006716949.3		Intron			XP_006717012.1

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