Product Details

SNP ID

rs151062160

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:82982727 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGGTGACTTTTTGGAATTGGTCC[C/T]GGTTAGATTGGTAATGGATCTGCTG

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	2414	Missense Mutation	AGG,GGG	R725G	NP_689786.2
XM_005251730.3	2414	Missense Mutation	AGG,GGG	R702G	XP_005251787.1
XM_005251731.3	2414	Missense Mutation	AGG,GGG	R596G	XP_005251788.1

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