Product Details

SNP ID
rs930122
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:53085313 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCTGGCCCCTGCCAGCCTCACAG[C/T]GAGGCAGCCTCCAGGCACCACCTCC
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 1813 Intron NP_443091.1
XM_005265537.4 1813 Intron XP_005265594.1
XM_006713384.3 1813 UTR 3 XP_006713447.1
XM_011534214.2 1813 Intron XP_011532516.1
XM_011534215.2 1813 Intron XP_011532517.1
XM_011534216.2 1813 Intron XP_011532518.1
XM_017007460.1 1813 Intron XP_016862949.1
XM_017007461.1 1813 Intron XP_016862950.1

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