Product Details

SNP ID

rs10403272

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:19078507 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAGACTCTGTGCATATGGTCATCC[C/T]TGTGTGGGTCATTTGCAGTACCGAT

Phenotype

MIM: 610823

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC25A42 PubMed Links

Gene Details

Gene

SLC25A42

Gene Name

solute carrier family 25 member 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321544.1		Intron			NP_001308473.1
NM_178526.4		Intron			NP_848621.2
XM_005259861.3		Intron			XP_005259918.1
XM_011527937.2		Intron			XP_011526239.1
XM_017026670.1		Intron			XP_016882159.1

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