Product Details

SNP ID

rs145514203

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:108623248 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCTCGGTGGGGGAGTAATTACGCA[C/T]GGGGTACATGTGGCCCTTGCGGGAG

Phenotype

MIM: 600738

Polymorphism

C/T, Transition 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	1285	Missense Mutation			NP_001193538.1
NM_003006.4	1285	Missense Mutation			NP_002997.2

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