Product Details

SNP ID
rs10793060
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:73409608 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCTGTTGGGCTGGACGACCGTGGT[A/G]TGGTGGATGACATGAGGCTGGGCAG
Phenotype
MIM: 616316
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM168A PubMed Links

Gene Details

Gene
FAM168A
Gene Name
family with sequence similarity 168 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286050.1 366 Silent Mutation CAC,CAT H167H NP_001272979.1
NM_001286051.1 366 Intron NP_001272980.1
NM_015159.2 366 Silent Mutation CAC,CAT H158H NP_055974.1
XM_017017415.1 366 Silent Mutation CAC,CAT H116H XP_016872904.1
XM_017017416.1 366 Intron XP_016872905.1

View Full Product Details