Product Details

SNP ID
rs11798996
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:49251014 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCCAGCCCTGAAGTAATCTGTG[C/T]GAGCAGCTGAGGCAGGCTCTGTGTG
Phenotype
MIM: 300859 MIM: 300292
Polymorphism
C/T, 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 1804 Intron NP_054727.1
XM_005272599.3 1804 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 1804 UTR 3 NP_001107849.1
NM_014009.3 1804 UTR 3 NP_054728.2
XM_006724533.2 1804 UTR 3 XP_006724596.2
XM_011543916.2 1804 UTR 3 XP_011542218.1
XM_017029565.1 1804 UTR 3 XP_016885054.1
XM_017029566.1 1804 UTR 3 XP_016885055.1
XM_017029567.1 1804 UTR 3 XP_016885056.1

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