Product Details

SNP ID

rs190269143

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:108623246 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATCTCGGTGGGGGAGTAATTACG[A/C]ACGGGGTACATGTGGCCCTTGCGGG

Phenotype

MIM: 600738

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SELPLG PubMed Links

Gene Details

Gene

SELPLG

Gene Name

selectin P ligand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206609.1	1287	Silent Mutation	GTG,GTT	V370V	NP_001193538.1
NM_003006.4	1287	Silent Mutation	GTG,GTT	V354V	NP_002997.2

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