Product Details

SNP ID
rs28489209
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:48902333 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACTAGACAGGGGCCACGACAAGTC[A/T]GACCGGGGCCACGACAAGTCTGACA
Phenotype
MIM: 300463 MIM: 314375 MIM: 300249
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
PQBP1 PubMed Links

Gene Details

Gene
PQBP1
Gene Name
polyglutamine binding protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001032381.1 472 Silent Mutation TCA,TCT S131S NP_001027553.1
NM_001032382.1 472 Silent Mutation TCA,TCT S131S NP_001027554.1
NM_001032383.1 472 Silent Mutation TCA,TCT S131S NP_001027555.1
NM_001032384.1 472 Silent Mutation TCA,TCT S131S NP_001027556.1
NM_001167989.1 472 Silent Mutation TCA,TCT S131S NP_001161461.1
NM_001167990.1 472 Silent Mutation TCA,TCT S123S NP_001161462.1
NM_001167992.1 472 Intron NP_001161464.1
NM_005710.2 472 Silent Mutation TCA,TCT S131S NP_005701.1
NM_144495.2 472 Intron NP_652766.1
XM_005272571.3 472 Silent Mutation TCA,TCT S131S XP_005272628.1
XM_005272572.4 472 Intron XP_005272629.1
XM_011543884.2 472 Silent Mutation TCA,TCT S131S XP_011542186.1
XM_017029207.1 472 Silent Mutation TCA,TCT S131S XP_016884696.1
Gene
SLC35A2
Gene Name
solute carrier family 35 member A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001032289.2 472 Intron NP_001027460.1
NM_001042498.2 472 Intron NP_001035963.1
NM_001282647.1 472 Intron NP_001269576.1
NM_001282648.1 472 Intron NP_001269577.1
NM_001282649.1 472 Intron NP_001269578.1
NM_001282650.1 472 Intron NP_001269579.1
NM_001282651.1 472 Intron NP_001269580.1
NM_005660.2 472 Intron NP_005651.1
Gene
TIMM17B
Gene Name
translocase of inner mitochondrial membrane 17 homolog B (yeast)
There are no transcripts associated with this gene.

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