Product Details

SNP ID
rs114750928
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:59752224 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGACGAAATGCAGTCTTTACCTG[C/T]GTCACTGAAAGTAGACCCGCAGAGC
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_001166243.2 867 UTR 3 NP_001159715.1
NM_001320899.1 867 UTR 3 NP_001307828.1
NM_001320900.1 867 UTR 3 NP_001307829.1
NM_001320901.1 867 UTR 3 NP_001307830.1
NM_002012.3 867 UTR 3 NP_002003.1
XM_017005880.1 867 Missense Mutation ACA,GCA T166A XP_016861369.1
XM_017005881.1 867 Missense Mutation ACA,GCA T166A XP_016861370.1
XM_017005882.1 867 Missense Mutation ACA,GCA T161A XP_016861371.1
XM_017005883.1 867 Missense Mutation ACA,GCA T166A XP_016861372.1
XM_017005884.1 867 Missense Mutation ACA,GCA T166A XP_016861373.1
XM_017005885.1 867 Missense Mutation ACA,GCA T85A XP_016861374.1
XM_017005886.1 867 Missense Mutation ACA,GCA T85A XP_016861375.1

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