Product Details

SNP ID

rs151252642

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:17486674 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGTGCAGCGACAGCCCGAGCGCCT[A/G]GCGCTGGTGGATGCCGGGACCGGCG

Phenotype

MIM: 600691

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC27A1 PubMed Links

Gene Details

Gene

SLC27A1

Gene Name

solute carrier family 27 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198580.2	316	Silent Mutation	CTA,CTG	L93L	NP_940982.1
XM_011528000.1	316	Silent Mutation	CTA,CTG	L93L	XP_011526302.1
XM_011528001.2	316	Silent Mutation	CTA,CTG	L93L	XP_011526303.1
XM_011528002.2	316	Silent Mutation	CTA,CTG	L93L	XP_011526304.1
XM_011528003.2	316	Silent Mutation	CTA,CTG	L93L	XP_011526305.1
XM_017026781.1	316	Silent Mutation	CTA,CTG	L93L	XP_016882270.1

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