Product Details

SNP ID
rs200614366
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:93728258 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACAAGCAGAAGATGATGAGGATGA[C/G]GAGTTAGATGTTACAGAAGAAGAAA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM92A1 PubMed Links

Gene Details

Gene
FAM92A1
Gene Name
family with sequence similarity 92 member A1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001283034.1 8313 Intron NP_001269963.1
NM_145269.4 8313 Intron NP_660312.2
XM_005250787.2 8313 Missense Mutation GAC,GAG D207E XP_005250844.1
Gene
RBM12B
Gene Name
RNA binding motif protein 12B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_203390.2 8313 Intron NP_976324.2
XM_005250915.4 8313 UTR 3 XP_005250972.1
XM_011517027.2 8313 UTR 3 XP_011515329.1
XM_011517028.2 8313 UTR 3 XP_011515330.1
XM_011517029.2 8313 UTR 3 XP_011515331.1
XM_017013406.1 8313 UTR 3 XP_016868895.1
XM_017013407.1 8313 UTR 3 XP_016868896.1
XM_017013408.1 8313 UTR 3 XP_016868897.1

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