Product Details

SNP ID
rs148953804
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:59752242 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTACCTGTGTCACTGAAAGTAGACC[C/T]GCAGAGCTGCGGCTTCTGCTGCCAT
Phenotype
MIM: 601153
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FHIT PubMed Links

Gene Details

Gene
FHIT
Gene Name
fragile histidine triad
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166243.2 849 Missense Mutation NP_001159715.1
NM_001320899.1 849 Missense Mutation NP_001307828.1
NM_001320900.1 849 Missense Mutation NP_001307829.1
NM_001320901.1 849 Missense Mutation NP_001307830.1
NM_002012.3 849 Missense Mutation NP_002003.1
XM_017005880.1 849 Missense Mutation XP_016861369.1
XM_017005881.1 849 Missense Mutation XP_016861370.1
XM_017005882.1 849 Missense Mutation XP_016861371.1
XM_017005883.1 849 Missense Mutation XP_016861372.1
XM_017005884.1 849 Missense Mutation XP_016861373.1
XM_017005885.1 849 Missense Mutation XP_016861374.1
XM_017005886.1 849 Missense Mutation XP_016861375.1

View Full Product Details