Product Details

SNP ID
rs150221272
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:82982750 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGGTTAGATTGGTAATGGATCTG[C/T]TGTCATCCTTGTCAGTTCTCTTTTT
Phenotype
MIM: 611344
Polymorphism
C/T, Transition 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 2391 Missense Mutation AAC,AGC N717S NP_689786.2
XM_005251730.3 2391 Missense Mutation AAC,AGC N694S XP_005251787.1
XM_005251731.3 2391 Missense Mutation AAC,AGC N588S XP_005251788.1

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