Product Details

SNP ID
rs10126690
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:93692673 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATCATTGCTTCCCTAAGGATCCTG[C/T]AGACTAGGTAGTAGTTATGTGCTGC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM133A PubMed Links

Gene Details

Gene
FAM133A
Gene Name
family with sequence similarity 133 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001171109.1 Intron NP_001164580.1
NM_001171110.1 Intron NP_001164581.1
NM_001171111.1 Intron NP_001164582.1
NM_173698.2 Intron NP_775969.1
XM_006724641.3 Intron XP_006724704.1
XM_011530925.2 Intron XP_011529227.1
XM_011530926.2 Intron XP_011529228.1
XM_011530927.2 Intron XP_011529229.1
XM_011530928.1 Intron XP_011529230.1
XM_011530929.1 Intron XP_011529231.1
XM_011530931.2 Intron XP_011529233.1
XM_017029454.1 Intron XP_016884943.1
XM_017029455.1 Intron XP_016884944.1
XM_017029456.1 Intron XP_016884945.1

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