Product Details

SNP ID
rs41265234
Assay Type
Functionally tested
NCBI dbSNP Submissions
21
Location
Chr.1:173803192 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAATGTCCAGACTTTGAGGGCTA[C/G]AGGGTACAGACCAAAGAAATTCAGT
Phenotype
MIM: 611503
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CENPL PubMed Links

Gene Details

Gene
CENPL
Gene Name
centromere protein L
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127181.2 1337 Missense Mutation TCT,TGT S291C NP_001120653.1
NM_001171182.1 1337 Missense Mutation TCT,TGT S245C NP_001164653.1
NM_033319.3 1337 Missense Mutation TCT,TGT S245C NP_201576.1

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