Product Details

SNP ID

rs146415600

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:58498570 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGTACATTTCTGCCGTCAGGGGC[C/T]GGAAGGACTGGGCCCGGTTGTCCAG

Phenotype

MIM: 603314

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC27A5 PubMed Links

Gene Details

Gene

SLC27A5

Gene Name

solute carrier family 27 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321196.1	2128	Missense Mutation	CAG,CGG	Q589R	NP_001308125.1
NM_012254.2	2128	Missense Mutation	CAG,CGG	Q673R	NP_036386.1
XM_011526364.1	2128	UTR 3			XP_011524666.1
XM_017026214.1	2128	Intron			XP_016881703.1

Gene

ZNF446

Gene Name

zinc finger protein 446

There are no transcripts associated with this gene.

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