Product Details

SNP ID
rs151146209
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:205771499 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTGGCCAAGAGCAGGCAGGGCAC[C/T]GGCTCTCCATTGGGTAGTGTGAGCT
Phenotype
MIM: 603949
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RAB29 PubMed Links

Gene Details

Gene
RAB29
Gene Name
RAB29, member RAS oncogene family
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135662.1 297 Silent Mutation CCA,CCG P117P NP_001129134.1
NM_001135663.1 297 Silent Mutation CCA,CCG P93P NP_001129135.1
NM_001135664.1 297 Silent Mutation CCA,CCG P45P NP_001129136.1
NM_003929.2 297 Silent Mutation CCA,CCG P117P NP_003920.1
XM_005245569.1 297 Silent Mutation CCA,CCG P117P XP_005245626.1
XM_005245570.1 297 Silent Mutation CCA,CCG P117P XP_005245627.1
XM_005245571.1 297 Silent Mutation CCA,CCG P117P XP_005245628.1
XM_006711605.3 297 Silent Mutation CCA,CCG P45P XP_006711668.1
XM_006711606.2 297 Silent Mutation CCA,CCG P45P XP_006711669.1
XM_017002748.1 297 Silent Mutation CCA,CCG P93P XP_016858237.1
XM_017002749.1 297 Silent Mutation CCA,CCG P93P XP_016858238.1
XM_017002750.1 297 Silent Mutation CCA,CCG P93P XP_016858239.1

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