Product Details

SNP ID
rs112081066
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:126556837 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTTGGCACCCACGTGCGCCAGCG[A/C]GTTGCGCACCACGGCGCTGGAGCTT
Phenotype
MIM: 609483
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
FAM84B PubMed Links

Gene Details

Gene
FAM84B
Gene Name
family with sequence similarity 84 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_174911.4 1082 Missense Mutation GCG,TCG A185S NP_777571.1
XM_017013107.1 1082 Missense Mutation GCG,TCG A185S XP_016868596.1
XM_017013108.1 1082 Missense Mutation GCG,TCG A167S XP_016868597.1

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