Product Details

SNP ID
rs201365495
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:153642419 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGAACCCTACTTAGGGGCGGGAT[A/G]TCACTCCGAGGTCAGTGCTGTGTAC
Phenotype
MIM: 614206 MIM: 601989
Polymorphism
A/G, Transition 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_001206612.1 772 Missense Mutation ATA,ATG I132M NP_001193541.1
NM_001244664.1 772 Intron NP_001231593.1
NM_001317077.1 772 Missense Mutation ATA,ATG I131M NP_001304006.1
NM_015607.3 772 Missense Mutation ATA,ATG I131M NP_056422.2
XM_017000993.1 772 Missense Mutation ATA,ATG I132M XP_016856482.1
Gene
S100A13
Gene Name
S100 calcium binding protein A13
There are no transcripts associated with this gene.

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