Product Details

SNP ID

rs201986043

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:13010445 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCATCGAGCTCGACGGGTCCAGAC[C/G]GGGAGAGGAGCCAGAAGAGGTGGCG

Phenotype

MIM: 614713

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RASSF10 PubMed Links

Gene Details

Gene

RASSF10

Gene Name

Ras association domain family member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080521.2	1023	Missense Mutation	CCG,CGG	P290R	NP_001073990.2

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