Product Details

SNP ID
rs143869281
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:49253921 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGTGCAAGGACCATTCTTACCTGG[G/T]AATGTGCTGTTTCCATGGCTACCCC
Phenotype
MIM: 300859 MIM: 300292
Polymorphism
G/T, Transversion 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 1151 Missense Mutation TTA,TTC L286F NP_001107849.1
NM_014009.3 1151 Missense Mutation TTA,TTC L321F NP_054728.2
XM_006724533.2 1151 Missense Mutation TTA,TTC L344F XP_006724596.2
XM_011543916.2 1151 Missense Mutation TTA,TTC L394F XP_011542218.1
XM_017029565.1 1151 Missense Mutation TTA,TTC L406F XP_016885054.1
XM_017029566.1 1151 Missense Mutation TTA,TTC L394F XP_016885055.1
XM_017029567.1 1151 Missense Mutation TTA,TTC L303F XP_016885056.1

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