Product Details

SNP ID

rs140964886

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:82982741 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAATTGGTCCCGGTTAGATTGGTA[A/C]TGGATCTGCTGTCATCCTTGTCAGT

Phenotype

MIM: 611344

Polymorphism

A/C, 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	2400	Missense Mutation	AGT,ATT	S720I	NP_689786.2
XM_005251730.3	2400	Missense Mutation	AGT,ATT	S697I	XP_005251787.1
XM_005251731.3	2400	Missense Mutation	AGT,ATT	S591I	XP_005251788.1

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