Product Details

SNP ID
rs540977901
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:95790666 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAGCACGAGAACCTAGACCGCCCC[A/C]GAAGTGCGGAGACCCCCTGGGCAGG
Phenotype
MIM: 607951
Polymorphism
A/C, Transversion 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_001243776.1 206 UTR 5 NP_001230705.1
NM_001243777.1 206 UTR 5 NP_001230706.1
NM_014679.4 206 UTR 5 NP_055494.2
XM_006718945.2 206 UTR 5 XP_006719008.1
XM_006718946.2 206 UTR 5 XP_006719009.1
XM_017018592.1 206 Intron XP_016874081.1
XM_017018593.1 206 UTR 5 XP_016874082.1
XM_017018594.1 206 UTR 5 XP_016874083.1
Gene
FAM76B
Gene Name
family with sequence similarity 76 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144664.4 206 Intron NP_653265.3
XM_005273775.4 206 Intron XP_005273832.1
XM_005273776.4 206 Intron XP_005273833.1
XM_011542610.2 206 Intron XP_011540912.1
XM_011542611.2 206 Intron XP_011540913.1
XM_011542612.1 206 Intron XP_011540914.1
XM_011542613.1 206 Intron XP_011540915.1

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