Product Details

SNP ID
rs137856773
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:20447843 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAAGACCTGCGCAGCGACGAGCA[G/T]GTCCGCACAGAGCTGGCCCGCATGA
Phenotype
MIM: 165370
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
RHOB PubMed Links

Gene Details

Gene
RHOB
Gene Name
ras homolog family member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004040.3 773 Missense Mutation CAG,CAT Q126H NP_004031.1

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