Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCAGAATCCTTACCTGTTGAAGAG[A/G]GCCTGTCTTCCCAGGCCCACCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600849 MIM: 613814 | ||||||||||||||||||||
Literature Links: |
NCOR1 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 |
NCOR1 - nuclear receptor corepressor 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190438.1 | 8505 | Intron | NP_001177367.1 | |||
NM_001190440.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2272 | NP_001177369.1 | |
NM_006311.3 | 8505 | Missense Mutation | CCC,CTC | P,L 2375 | NP_006302.2 | |
XM_005256866.4 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_005256923.1 | |
XM_005256868.4 | 8505 | Missense Mutation | CCC,CTC | P,L 2458 | XP_005256925.1 | |
XM_005256871.4 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_005256928.1 | |
XM_005256872.4 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_005256929.1 | |
XM_005256873.4 | 8505 | Missense Mutation | CCC,CTC | P,L 2443 | XP_005256930.1 | |
XM_005256874.4 | 8505 | Missense Mutation | CCC,CTC | P,L 2401 | XP_005256931.1 | |
XM_005256875.3 | 8505 | Missense Mutation | CCC,CTC | P,L 2383 | XP_005256932.1 | |
XM_006721601.3 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_006721664.1 | |
XM_006721602.3 | 8505 | Missense Mutation | CCC,CTC | P,L 2458 | XP_006721665.1 | |
XM_006721603.3 | 8505 | Missense Mutation | CCC,CTC | P,L 2446 | XP_006721666.1 | |
XM_006721604.3 | 8505 | Missense Mutation | CCC,CTC | P,L 2391 | XP_006721667.1 | |
XM_011524083.2 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_011522385.1 | |
XM_011524084.2 | 8505 | Missense Mutation | CCC,CTC | P,L 2458 | XP_011522386.1 | |
XM_011524085.2 | 8505 | Missense Mutation | CCC,CTC | P,L 2340 | XP_011522387.1 | |
XM_011524086.2 | 8505 | Missense Mutation | CCC,CTC | P,L 2272 | XP_011522388.1 | |
XM_017025396.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_016880885.1 | |
XM_017025397.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_016880886.1 | |
XM_017025398.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_016880887.1 | |
XM_017025399.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2459 | XP_016880888.1 | |
XM_017025400.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2458 | XP_016880889.1 | |
XM_017025401.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2458 | XP_016880890.1 | |
XM_017025402.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2458 | XP_016880891.1 | |
XM_017025403.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_016880892.1 | |
XM_017025404.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_016880893.1 | |
XM_017025405.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_016880894.1 | |
XM_017025406.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_016880895.1 | |
XM_017025407.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_016880896.1 | |
XM_017025408.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2450 | XP_016880897.1 | |
XM_017025409.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_016880898.1 | |
XM_017025410.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_016880899.1 | |
XM_017025411.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_016880900.1 | |
XM_017025412.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_016880901.1 | |
XM_017025413.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_016880902.1 | |
XM_017025414.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2449 | XP_016880903.1 | |
XM_017025415.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2400 | XP_016880904.1 | |
XM_017025416.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2391 | XP_016880905.1 | |
XM_017025417.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2385 | XP_016880906.1 | |
XM_017025418.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2339 | XP_016880907.1 | |
XM_017025419.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2282 | XP_016880908.1 | |
XM_017025420.1 | 8505 | Missense Mutation | CCC,CTC | P,L 2266 | XP_016880909.1 |
TTC19 - tetratricopeptide repeat domain 19 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271420.1 | 8505 | Intron | NP_001258349.1 | |||
NM_017775.3 | 8505 | Intron | NP_060245.3 | |||
XM_017024801.1 | 8505 | Intron | XP_016880290.1 | |||
XM_017024802.1 | 8505 | Intron | XP_016880291.1 |