Product Details

SNP ID
rs979312
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:59751771 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGAAGAGTCCACTCAGTGAAAGCA[C/G]AGGAGTTTGCCCGGGGGCGTGTTAG
Phenotype
MIM: 601153
Polymorphism
C/G, Transversion 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 1987 Intron NP_001159715.1
NM_001320899.1 1987 UTR 3 NP_001307828.1
NM_001320900.1 1987 UTR 3 NP_001307829.1
NM_001320901.1 1987 UTR 3 NP_001307830.1
NM_002012.3 1987 Intron NP_002003.1
XM_017005880.1 1987 UTR 3 XP_016861369.1
XM_017005881.1 1987 UTR 3 XP_016861370.1
XM_017005882.1 1987 UTR 3 XP_016861371.1
XM_017005883.1 1987 Intron XP_016861372.1
XM_017005884.1 1987 Intron XP_016861373.1
XM_017005885.1 1987 UTR 3 XP_016861374.1
XM_017005886.1 1987 UTR 3 XP_016861375.1

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