Product Details

SNP ID
rs190518632
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:59749390 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACCTCAAATCTGCCTGTCTGAGCC[G/A]TTTAGGTCTAGGTATTTTAAGGGAG
Phenotype
MIM: 601153
Polymorphism
G/A, 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 1049 UTR 3 NP_001159715.1
NM_001320899.1 1049 UTR 3 NP_001307828.1
NM_001320900.1 1049 UTR 3 NP_001307829.1
NM_001320901.1 1049 UTR 3 NP_001307830.1
NM_002012.3 1049 UTR 3 NP_002003.1
XM_017005880.1 1049 UTR 3 XP_016861369.1
XM_017005881.1 1049 UTR 3 XP_016861370.1
XM_017005882.1 1049 UTR 3 XP_016861371.1
XM_017005883.1 1049 UTR 3 XP_016861372.1
XM_017005884.1 1049 UTR 3 XP_016861373.1
XM_017005885.1 1049 UTR 3 XP_016861374.1
XM_017005886.1 1049 UTR 3 XP_016861375.1

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