Product Details

SNP ID
rs551486752
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:130398806 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTCATGGTCTTTCCTCTGCAGAA[G/T]TTTCTGGAAATGACCCAACTTGGGA
Phenotype
MIM: 610523
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CEP41 PubMed Links

Gene Details

Gene
CEP41
Gene Name
centrosomal protein 41
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001257158.1 1412 UTR 3 NP_001244087.1
NM_001257159.1 1412 UTR 3 NP_001244088.1
NM_001257160.1 1412 Intron NP_001244089.1
NM_018718.2 1412 UTR 3 NP_061188.1
XM_011516709.2 1412 UTR 3 XP_011515011.1
XM_011516710.2 1412 UTR 3 XP_011515012.1

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