Product Details

SNP ID
rs117876788
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:95793788 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTTCTCTAGCTAGTAAATGACAGT[A/G]TCTTAATGGGCTTTGGATTTAATGG
Phenotype
MIM: 607951
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CEP57 PubMed Links

Gene Details

Gene
CEP57
Gene Name
centrosomal protein 57
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243776.1 684 Intron NP_001230705.1
NM_001243777.1 684 Intron NP_001230706.1
NM_014679.4 684 Intron NP_055494.2
XM_006718945.2 684 Intron XP_006719008.1
XM_006718946.2 684 Intron XP_006719009.1
XM_017018592.1 684 UTR 5 XP_016874081.1
XM_017018593.1 684 Intron XP_016874082.1
XM_017018594.1 684 Intron XP_016874083.1
Gene
FAM76B
Gene Name
family with sequence similarity 76 member B
There are no transcripts associated with this gene.

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