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SNP ID

rs765676628

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:169726637 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATCAGTAAGCAAGACCATGACTT[A/G]TCAATGAGAAAGAAATGTATTTTCA

Phenotype

MIM: 131210

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SELE PubMed Links

Gene Details

Gene

SELE

Gene Name

selectin E

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000450.2		Intron			NP_000441.2

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