Product Details

SNP ID
rs200447055
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:128672514 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCATTCTCCAGAATTCAATTTGTT[C/T]TCCAACTCGGTGGTGTTTGAAAGCA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM71F2 PubMed Links

Gene Details

Gene
FAM71F2
Gene Name
family with sequence similarity 71 member F2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001012454.5 249 Silent Mutation TTC,TTT F39F NP_001012457.3
NM_001128926.3 249 Silent Mutation TTC,TTT F39F NP_001122398.1
NM_001290254.1 249 UTR 5 NP_001277183.1
NM_001290255.1 249 UTR 5 NP_001277184.1
XM_011516128.2 249 Silent Mutation TTC,TTT F39F XP_011514430.1
XM_011516129.2 249 Silent Mutation TTC,TTT F39F XP_011514431.1
XM_011516130.2 249 Silent Mutation TTC,TTT F39F XP_011514432.1
XM_011516131.2 249 Silent Mutation TTC,TTT F39F XP_011514433.1
XM_011516132.2 249 Silent Mutation TTC,TTT F39F XP_011514434.1
XM_011516134.2 249 UTR 5 XP_011514436.1
XM_011516135.2 249 Intron XP_011514437.1
XM_011516136.2 249 Intron XP_011514438.1
XM_017012147.1 249 UTR 5 XP_016867636.1
XM_017012149.1 249 Silent Mutation TTC,TTT F39F XP_016867638.1

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