Product Details

SNP ID
rs201207581
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:46326454 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAGACGGCGAAGAGGAAGGGCTC[C/G]GCTGTCGATGCGTCTGTCCAGGAGG
Phenotype
MIM: 605925
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C21orf58 PubMed Links

Gene Details

Gene
C21orf58
Gene Name
chromosome 21 open reading frame 58
There are no transcripts associated with this gene.

Gene
PCNT
Gene Name
pericentrin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001315529.1 427 UTR 5 NP_001302458.1
NM_006031.5 427 Silent Mutation TCC,TCG S44S NP_006022.3
XM_005261124.4 427 Silent Mutation TCC,TCG S44S XP_005261181.1
XM_011529594.2 427 Silent Mutation TCC,TCG S44S XP_011527896.1
XM_017028362.1 427 Silent Mutation TCC,TCG S44S XP_016883851.1
XM_017028363.1 427 UTR 5 XP_016883852.1

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