Product Details

SNP ID

rs202102875

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128345210 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGGTGCGACAGTGCCTGCAGGAG[C/T]GGCGGACAGTGCCCATTTTGTTTGC

Phenotype

MIM: 604194

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC27A4 PubMed Links

Gene Details

Gene

SLC27A4

Gene Name

solute carrier family 27 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005094.3	375	Missense Mutation	CGG,TGG	R73W	NP_005085.2
XM_017014222.1	375	Missense Mutation	CGG,TGG	R73W	XP_016869711.1

View Full Product Details