Product Details

SNP ID
rs122467175
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:49251711 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAAGAAGGCAAACATGCGTGTGA[G/A]CCAGTGGTAGATCTCATTGAGTGTC
Phenotype
MIM: 300859 MIM: 300292
Polymorphism
G/A, Transition substitution
Allele Nomenclature
Literature Links
CCDC22 PubMed Links

Gene Details

Gene
CCDC22
Gene Name
coiled-coil domain containing 22
There are no transcripts associated with this gene.

Gene
FOXP3
Gene Name
forkhead box P3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114377.1 1287 Missense Mutation CTC,TTC L332F NP_001107849.1
NM_014009.3 1287 Missense Mutation CTC,TTC L367F NP_054728.2
XM_006724533.2 1287 Missense Mutation CTC,TTC L390F XP_006724596.2
XM_011543916.2 1287 Missense Mutation CTC,TTC L440F XP_011542218.1
XM_017029565.1 1287 Missense Mutation CTC,TTC L452F XP_016885054.1
XM_017029566.1 1287 Missense Mutation CTC,TTC L440F XP_016885055.1
XM_017029567.1 1287 Missense Mutation CTC,TTC L349F XP_016885056.1

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