Product Details

SNP ID
rs11021313
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:95773743 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTACACAGAAGGCACTCAAATGTTA[C/G]GTCCCTTTTCCTTTTAACCACTTAC
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
FAM76B PubMed Links

Gene Details

Gene
FAM76B
Gene Name
family with sequence similarity 76 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144664.4 Intron NP_653265.3
XM_005273775.4 Intron XP_005273832.1
XM_005273776.4 Intron XP_005273833.1
XM_011542610.2 Intron XP_011540912.1
XM_011542611.2 Intron XP_011540913.1
XM_011542612.1 Intron XP_011540914.1
XM_011542613.1 Intron XP_011540915.1

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