Product Details

SNP ID
rs145431546
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:153638316 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGCTTTACTAATATGCTGAAGAA[C/G]AAACAGCCGACGCCAGTGAATATTC
Phenotype
MIM: 614206 MIM: 176940 MIM: 601989
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CHTOP PubMed Links

Gene Details

Gene
CHTOP
Gene Name
chromatin target of PRMT1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206612.1 466 Missense Mutation AAC,AAG N29K NP_001193541.1
NM_001244664.1 466 Missense Mutation AAC,AAG N29K NP_001231593.1
NM_001317077.1 466 Missense Mutation AAC,AAG N29K NP_001304006.1
NM_015607.3 466 Missense Mutation AAC,AAG N29K NP_056422.2
XM_017000993.1 466 Missense Mutation AAC,AAG N29K XP_016856482.1
Gene
S100A1
Gene Name
S100 calcium binding protein A1
There are no transcripts associated with this gene.

Gene
S100A13
Gene Name
S100 calcium binding protein A13
There are no transcripts associated with this gene.

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