Product Details

SNP ID
rs74343948
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:128672409 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTACCAAGAACCAATGAGTAAAAT[C/G]AGGGGCCTCCCACCTGAGGTCAGGG
Phenotype
Polymorphism
C/G, Transversion 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_001012454.5 144 Missense Mutation ATC,ATG I4M NP_001012457.3
NM_001128926.3 144 Missense Mutation ATC,ATG I4M NP_001122398.1
NM_001290254.1 144 UTR 5 NP_001277183.1
NM_001290255.1 144 UTR 5 NP_001277184.1
XM_011516128.2 144 Missense Mutation ATC,ATG I4M XP_011514430.1
XM_011516129.2 144 Missense Mutation ATC,ATG I4M XP_011514431.1
XM_011516130.2 144 Missense Mutation ATC,ATG I4M XP_011514432.1
XM_011516131.2 144 Missense Mutation ATC,ATG I4M XP_011514433.1
XM_011516132.2 144 Missense Mutation ATC,ATG I4M XP_011514434.1
XM_011516134.2 144 Intron XP_011514436.1
XM_011516135.2 144 Intron XP_011514437.1
XM_011516136.2 144 Intron XP_011514438.1
XM_017012147.1 144 UTR 5 XP_016867636.1
XM_017012149.1 144 Missense Mutation ATC,ATG I4M XP_016867638.1

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