Product Details

SNP ID
rs11613325
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:132843252 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTCTGAGATTTCAGGAAAGGAAAC[A/G]CATGTTTAACTAAAAACCCAACTGA
Phenotype
MIM: 605209
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CHFR PubMed Links

Gene Details

Gene
CHFR
Gene Name
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001161344.1 Intron NP_001154816.1
NM_001161345.1 Intron NP_001154817.1
NM_001161346.1 Intron NP_001154818.1
NM_001161347.1 Intron NP_001154819.1
NM_018223.2 Intron NP_060693.2

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