Product Details
- SNP ID
-
rs138200388
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:16032412 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTTGGTTCACCGCAGAGGGAGCAC[A/G]TGCAATCGGTGTTGGTGGAGTACTG
- Phenotype
-
MIM: 600849
MIM: 613814
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NCOR1
PubMed Links
Gene Details
- Gene
- NCOR1
- Gene Name
- nuclear receptor corepressor 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001190438.1 |
8588 |
Intron |
|
|
NP_001177367.1 |
NM_001190440.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2300C |
NP_001177369.1 |
NM_006311.3 |
8588 |
Missense Mutation |
CGT,TGT |
R2403C |
NP_006302.2 |
XM_005256866.4 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_005256923.1 |
XM_005256868.4 |
8588 |
Missense Mutation |
CGT,TGT |
R2486C |
XP_005256925.1 |
XM_005256871.4 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_005256928.1 |
XM_005256872.4 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_005256929.1 |
XM_005256873.4 |
8588 |
Missense Mutation |
CGT,TGT |
R2471C |
XP_005256930.1 |
XM_005256874.4 |
8588 |
Missense Mutation |
CGT,TGT |
R2429C |
XP_005256931.1 |
XM_005256875.3 |
8588 |
Missense Mutation |
CGT,TGT |
R2411C |
XP_005256932.1 |
XM_006721601.3 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_006721664.1 |
XM_006721602.3 |
8588 |
Missense Mutation |
CGT,TGT |
R2486C |
XP_006721665.1 |
XM_006721603.3 |
8588 |
Missense Mutation |
CGT,TGT |
R2474C |
XP_006721666.1 |
XM_006721604.3 |
8588 |
Missense Mutation |
CGT,TGT |
R2419C |
XP_006721667.1 |
XM_011524083.2 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_011522385.1 |
XM_011524084.2 |
8588 |
Missense Mutation |
CGT,TGT |
R2486C |
XP_011522386.1 |
XM_011524085.2 |
8588 |
Missense Mutation |
CGT,TGT |
R2368C |
XP_011522387.1 |
XM_011524086.2 |
8588 |
Missense Mutation |
CGT,TGT |
R2300C |
XP_011522388.1 |
XM_017025396.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_016880885.1 |
XM_017025397.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_016880886.1 |
XM_017025398.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_016880887.1 |
XM_017025399.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2487C |
XP_016880888.1 |
XM_017025400.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2486C |
XP_016880889.1 |
XM_017025401.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2486C |
XP_016880890.1 |
XM_017025402.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2486C |
XP_016880891.1 |
XM_017025403.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_016880892.1 |
XM_017025404.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_016880893.1 |
XM_017025405.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_016880894.1 |
XM_017025406.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_016880895.1 |
XM_017025407.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_016880896.1 |
XM_017025408.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2478C |
XP_016880897.1 |
XM_017025409.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_016880898.1 |
XM_017025410.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_016880899.1 |
XM_017025411.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_016880900.1 |
XM_017025412.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_016880901.1 |
XM_017025413.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_016880902.1 |
XM_017025414.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2477C |
XP_016880903.1 |
XM_017025415.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2428C |
XP_016880904.1 |
XM_017025416.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2419C |
XP_016880905.1 |
XM_017025417.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2413C |
XP_016880906.1 |
XM_017025418.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2367C |
XP_016880907.1 |
XM_017025419.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2310C |
XP_016880908.1 |
XM_017025420.1 |
8588 |
Missense Mutation |
CGT,TGT |
R2294C |
XP_016880909.1 |
- Gene
- TTC19
- Gene Name
- tetratricopeptide repeat domain 19
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