Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAACACCTGCTGGGCCTCTGGCTCC[A/G]TTTCTTGCGGAACTCCAGCTCATCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300859 MIM: 300292 | ||||||||||||||||||||
Literature Links: |
CCDC22 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CCDC22 - coiled-coil domain containing 22 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014008.4 | 1437 | Intron | NP_054727.1 | |||
XM_005272599.3 | 1437 | Intron | XP_005272656.1 |
FOXP3 - forkhead box P3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114377.1 | 1437 | Missense Mutation | CGG,TGG | R,W 382 | NP_001107849.1 | |
NM_014009.3 | 1437 | Missense Mutation | CGG,TGG | R,W 417 | NP_054728.2 | |
XM_006724533.2 | 1437 | Missense Mutation | CGG,TGG | R,W 440 | XP_006724596.2 | |
XM_011543916.2 | 1437 | Missense Mutation | CGG,TGG | R,W 550 | XP_011542218.1 | |
XM_017029565.1 | 1437 | Missense Mutation | CGG,TGG | R,W 502 | XP_016885054.1 | |
XM_017029566.1 | 1437 | Missense Mutation | CGG,TGG | R,W 490 | XP_016885055.1 | |
XM_017029567.1 | 1437 | Missense Mutation | CGG,TGG | R,W 459 | XP_016885056.1 |