Product Details

SNP ID

rs12758669

Assay Type

Functionally tested

NCBI dbSNP Submissions

9

Location

Chr.1:169691575 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGACAAAAAGCTGAGCTGTATAAA[C/G]ACCTGTGGGCTGGGGGTTGAGGGAT

Phenotype

MIM: 153240

Polymorphism

C/G, Transversion 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	1532	UTR 3			NP_000646.2

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