Product Details

SNP ID
rs122467169
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:49251698 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAGGATGGTTTCTGAAGAAGGCA[C/A]ACATGCGTGTGAACCAGTGGTAGAT
Phenotype
MIM: 300859 MIM: 300292
Polymorphism
C/A, 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 1300 Missense Mutation TGT,TTT C336F NP_001107849.1
NM_014009.3 1300 Missense Mutation TGT,TTT C371F NP_054728.2
XM_006724533.2 1300 Missense Mutation TGT,TTT C394F XP_006724596.2
XM_011543916.2 1300 Missense Mutation TGT,TTT C444F XP_011542218.1
XM_017029565.1 1300 Missense Mutation TGT,TTT C456F XP_016885054.1
XM_017029566.1 1300 Missense Mutation TGT,TTT C444F XP_016885055.1
XM_017029567.1 1300 Missense Mutation TGT,TTT C353F XP_016885056.1

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