Product Details

SNP ID

rs201871582

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:102228463 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGGGCATTATGGGGACTGTGCTA[C/T]TTACCGGGGGCCTAAAGCAAACCGT

Phenotype

MIM: 611815 MIM: 602669

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ELOVL3 PubMed Links

Gene Details

Gene

ELOVL3

Gene Name

ELOVL fatty acid elongase 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152310.2	1541	Missense Mutation	CTT,TTT	L94F	NP_689523.1
XM_011540245.2	1541	Missense Mutation	CTT,TTT	L94F	XP_011538547.1

Gene

PITX3

Gene Name

paired like homeodomain 3

There are no transcripts associated with this gene.

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