Product Details

SNP ID

rs61762487

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:108623389 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTGGTCTGGGGCCCCCACTGGGT[G/A]GTTGACGGACAAATTGCTGGCTGCC

Phenotype

MIM: 600738

Polymorphism

G/A, 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	1144	Missense Mutation	CAC,TAC	H323Y	NP_001193538.1
NM_003006.4	1144	Missense Mutation	CAC,TAC	H307Y	NP_002997.2

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