Product Details

SNP ID

rs7873861

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:82980703 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCATCTACATATATCTGATCCAAT[C/G]TCATCAAAAGATGCCACTAAGACAA

Phenotype

MIM: 611344

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RASEF PubMed Links

Gene Details

Gene

RASEF

Gene Name

RAS and EF-hand domain containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152573.3	4438	UTR 3			NP_689786.2
XM_005251730.3	4438	UTR 3			XP_005251787.1
XM_005251731.3	4438	UTR 3			XP_005251788.1

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