Product Details

SNP ID
rs143868192
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:55718357 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGAATCTGACTCTGAGAAAACGAC[C/G]GAGAAAGAAAATCTGGGGCCGAGAA
Phenotype
MIM: 300725
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
RRAGB PubMed Links

Gene Details

Gene
RRAGB
Gene Name
Ras related GTP binding B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006064.4 637 Silent Mutation ACC,ACG T10T NP_006055.3
NM_016656.3 637 Silent Mutation ACC,ACG T10T NP_057740.2
XM_005261973.4 637 Intron XP_005262030.1
XM_017029217.1 637 Intron XP_016884706.1
XM_017029218.1 637 Silent Mutation ACC,ACG T10T XP_016884707.1

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