Product Details

SNP ID
rs4758909
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:132841203 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCCTTCTCCCTTGAAACTTTTCCT[A/G]AAAACAGACTTCTGCTTTAACTGTA
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 2307 UTR 3 NP_001154816.1
NM_001161345.1 2307 UTR 3 NP_001154817.1
NM_001161346.1 2307 UTR 3 NP_001154818.1
NM_001161347.1 2307 UTR 3 NP_001154819.1
NM_018223.2 2307 UTR 3 NP_060693.2

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