Product Details

SNP ID
rs28935477
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:49251441 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAGCCCCCTTCTCGCTCTCCACCC[A/G]CACAAAGCACTTGTGCAGACTCAGG
Phenotype
MIM: 300859 MIM: 300292
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CCDC22 PubMed Links

Gene Details

Gene
CCDC22
Gene Name
coiled-coil domain containing 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014008.4 1377 Intron NP_054727.1
XM_005272599.3 1377 Intron XP_005272656.1
Gene
FOXP3
Gene Name
forkhead box P3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114377.1 1377 Missense Mutation CGG,TGG R362W NP_001107849.1
NM_014009.3 1377 Missense Mutation CGG,TGG R397W NP_054728.2
XM_006724533.2 1377 Missense Mutation CGG,TGG R420W XP_006724596.2
XM_011543916.2 1377 Missense Mutation CGG,TGG R530W XP_011542218.1
XM_017029565.1 1377 Missense Mutation CGG,TGG R482W XP_016885054.1
XM_017029566.1 1377 Missense Mutation CGG,TGG R470W XP_016885055.1
XM_017029567.1 1377 Missense Mutation CGG,TGG R439W XP_016885056.1

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