Product Details

SNP ID
rs200660955
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:95396126 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGTTTTAGGTAAGATTATCTCCA[A/G]CCAAAATGTCAACCAAGAATTCTAC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM81B PubMed Links

Gene Details

Gene
FAM81B
Gene Name
family with sequence similarity 81 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152548.2 313 Missense Mutation ACC,GCC T82A NP_689761.2
XM_005271905.2 313 UTR 5 XP_005271962.2
XM_005271906.4 313 UTR 5 XP_005271963.2
XM_005271907.3 313 Missense Mutation ACC,GCC T82A XP_005271964.1
XM_011543207.1 313 Missense Mutation ACC,GCC T82A XP_011541509.1
XM_011543208.1 313 Missense Mutation ACC,GCC T82A XP_011541510.1
XM_011543209.1 313 Intron XP_011541511.1
XM_011543210.2 313 Intron XP_011541512.1
XM_017009118.1 313 UTR 5 XP_016864607.1

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