Product Details

SNP ID

rs190346554

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:37903389 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGCCGTAGCGCTGGGCGCCCTCCA[C/T]TACCTGGCACTTTTCCTGCAACTCG

Phenotype

MIM: 616537

Polymorphism

C/T, 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	293	Silent Mutation	CAC,CAT	H13H	NP_542174.1
XM_011528530.1	293	Silent Mutation	CAC,CAT	H13H	XP_011526832.1

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