Product Details

SNP ID

rs139716647

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:108623095 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAGGGAGGAAGCTGTGCAGGGTGA[A/G]GTCATCCCCCTCACGGTCCTCCCTG

Phenotype

MIM: 600738

Polymorphism

A/G, 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	1438	Missense Mutation	CTC,TTC	L421F	NP_001193538.1
NM_003006.4	1438	Missense Mutation	CTC,TTC	L405F	NP_002997.2

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