Product Details

SNP ID

rs4987370

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:169693384 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGGGTCTTGAGTTCTAAAAGCATA[C/T]GCGTTAAGAGCATGATTCCTGGATC

Phenotype

MIM: 153240

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SELL PubMed Links

Gene Details

Gene

SELL

Gene Name

selectin L

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000655.4		Intron			NP_000646.2

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