Product Details

SNP ID

hCV28012607

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:37744495 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCGTGTCTGTTGTAGCACCTTGG[A/T]AAAGGAGAGCTGCCGTGTCTGAGGG

Phenotype

MIM: 611605

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

ERLIN2 PubMed Links

Gene Details

Gene

ERLIN2

Gene Name

ER lipid raft associated 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003790.3		Intron			NP_001003790.1
NM_001003791.2		Intron			NP_001003791.1
NM_007175.6		Intron			NP_009106.1

Gene

LOC102723701

Gene Name

uncharacterized LOC102723701

There are no transcripts associated with this gene.

Gene

LOC728024

Gene Name

chromosome X open reading frame 56 pseudogene

There are no transcripts associated with this gene.

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