Product Details

SNP ID
rs188738478
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:54922592 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGTGTGTAGGGCCCTCTGCCTCC[C/T]CCGGGGAGCCTGGGGCTTCCCTTCC
Phenotype
MIM: 300132
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TRO PubMed Links

Gene Details

Gene
TRO
Gene Name
trophinin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039705.2 420 Silent Mutation CCC,CCT P20P NP_001034794.1
NM_001271183.1 420 Intron NP_001258112.1
NM_001271184.1 420 Intron NP_001258113.1
NM_016157.3 420 Silent Mutation CCC,CCT P20P NP_057241.2
NM_177556.2 420 Silent Mutation CCC,CCT P20P NP_808224.1
NM_177557.2 420 Intron NP_808225.1
XM_006724600.2 420 Silent Mutation CCC,CCT P20P XP_006724663.1
XM_011530808.1 420 Silent Mutation CCC,CCT P20P XP_011529110.1
XM_011530809.1 420 Silent Mutation CCC,CCT P20P XP_011529111.1
XM_011530811.2 420 Silent Mutation CCC,CCT P20P XP_011529113.1
XM_011530812.1 420 Silent Mutation CCC,CCT P20P XP_011529114.1
XM_011530813.1 420 Silent Mutation CCC,CCT P20P XP_011529115.1
XM_011530814.1 420 Intron XP_011529116.1
XM_017029767.1 420 Silent Mutation CCC,CCT P20P XP_016885256.1
XM_017029768.1 420 Intron XP_016885257.1
XM_017029769.1 420 Silent Mutation CCC,CCT P20P XP_016885258.1
XM_017029770.1 420 Silent Mutation CCC,CCT P20P XP_016885259.1
XM_017029771.1 420 Silent Mutation CCC,CCT P20P XP_016885260.1
XM_017029772.1 420 Intron XP_016885261.1
XM_017029773.1 420 Intron XP_016885262.1

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