Product Details

SNP ID
rs200331102
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:128672508 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACTGATTCATTCTCCAGAATTCAA[G/T]TTGTTCTCCAACTCGGTGGTGTTTG
Phenotype
Polymorphism
G/T, 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_001012454.5 243 Missense Mutation AAG,AAT K37N NP_001012457.3
NM_001128926.3 243 Missense Mutation AAG,AAT K37N NP_001122398.1
NM_001290254.1 243 UTR 5 NP_001277183.1
NM_001290255.1 243 UTR 5 NP_001277184.1
XM_011516128.2 243 Missense Mutation AAG,AAT K37N XP_011514430.1
XM_011516129.2 243 Missense Mutation AAG,AAT K37N XP_011514431.1
XM_011516130.2 243 Missense Mutation AAG,AAT K37N XP_011514432.1
XM_011516131.2 243 Missense Mutation AAG,AAT K37N XP_011514433.1
XM_011516132.2 243 Missense Mutation AAG,AAT K37N XP_011514434.1
XM_011516134.2 243 UTR 5 XP_011514436.1
XM_011516135.2 243 Intron XP_011514437.1
XM_011516136.2 243 Intron XP_011514438.1
XM_017012147.1 243 UTR 5 XP_016867636.1
XM_017012149.1 243 Missense Mutation AAG,AAT K37N XP_016867638.1

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