Product Details

SNP ID
rs4687700
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:53071522 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGGCCCCAGGTCACAGGGGCCGAC[C/T]TGGGACATAGAGAAAGATCCAGCCA
Phenotype
MIM: 611908
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RFT1 PubMed Links

Gene Details

Gene
RFT1
Gene Name
RFT1 homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052859.3 5266 Intron NP_443091.1
XM_005265537.4 5266 Intron XP_005265594.1
XM_006713384.3 5266 Intron XP_006713447.1
XM_011534214.2 5266 UTR 3 XP_011532516.1
XM_011534215.2 5266 UTR 3 XP_011532517.1
XM_011534216.2 5266 Intron XP_011532518.1
XM_017007460.1 5266 Intron XP_016862949.1
XM_017007461.1 5266 Intron XP_016862950.1

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