Product Details

SNP ID

rs6013414

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:37905969 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTTTAGCAGATTGGGGCCTGATC[A/G]TTTCATTATTCCTGGGCTCCGTGTG

Phenotype

MIM: 616537

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VSTM2L PubMed Links

Gene Details

Gene

VSTM2L

Gene Name

V-set and transmembrane domain containing 2 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080607.2		Intron			NP_542174.1
XM_011528530.1		Intron			XP_011526832.1

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