Product Details

SNP ID

rs5800

Assay Type

Functionally tested

NCBI dbSNP Submissions

51

Location

Chr.1:41479019 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCCAGCCTCAGGGGAGCCATCCAG[C/T]CTCCAGGGCTGGCTGAGGCATGCGT

Phenotype

MIM: 131241

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

EDN2 PubMed Links

Gene Details

Gene

EDN2

Gene Name

endothelin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302269.1	1009	UTR 3			NP_001289198.1
NM_001956.4	1009	UTR 3			NP_001947.1
XM_017000512.1	1009	UTR 3			XP_016856001.1

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