Product Details

SNP ID
rs114190003
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:134782098 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTCCACATAAACTCAATCAAAAA[C/G]TTGGCAGCCCTAAAAAACTTCTCAC
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM122B PubMed Links

Gene Details

Gene
FAM122B
Gene Name
family with sequence similarity 122B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166599.2 Intron NP_001160071.1
NM_001166600.2 Intron NP_001160072.1
NM_001170756.1 Intron NP_001164227.1
NM_001170757.1 Intron NP_001164228.1
NM_145284.5 Intron NP_660327.2
XM_006724730.2 Intron XP_006724793.1
XM_006724732.2 Intron XP_006724795.1
XM_006724733.3 Intron XP_006724796.1
XM_011531282.1 Intron XP_011529584.1
XM_011531283.1 Intron XP_011529585.1
XM_011531284.1 Intron XP_011529586.1
XM_011531285.1 Intron XP_011529587.1
XM_011531286.1 Intron XP_011529588.1
XM_011531287.1 Intron XP_011529589.1
XM_011531288.1 Intron XP_011529590.1
XM_011531289.1 Intron XP_011529591.1
XM_011531290.1 Intron XP_011529592.1
XM_011531291.1 Intron XP_011529593.1
XM_011531292.1 Intron XP_011529594.1
XM_011531293.1 Intron XP_011529595.1
XM_011531294.1 Intron XP_011529596.1
XM_017029306.1 Intron XP_016884795.1
XM_017029307.1 Intron XP_016884796.1

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