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- SNP ID:
- rs141252590
- Gene
-
CTBP2ZRANB1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.10: 124989691 - 124989691 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
CCTGGAGCCACACCCACGATGCCTG[A/G]CGGATATCTAAGGAACACACAGAAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602619
MIM: 611749
|
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Literature Links: |
CTBP2 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 |
| CTBP2 - C-terminal binding protein 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001083914.2 | 3373 | Intron | NP_001077383.1 | |||
| NM_001290214.2 | 3373 | Intron | NP_001277143.1 | |||
| NM_001290215.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | NP_001277144.1 | |
| NM_001321012.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | NP_001307941.1 | |
| NM_001321013.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | NP_001307942.1 | |
| NM_001321014.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | NP_001307943.1 | |
| NM_001329.3 | 3373 | Intron | NP_001320.1 | |||
| NM_022802.2 | 3373 | Missense Mutation | CCA,TCA | P,S 929 | NP_073713.2 | |
| XM_005269561.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269618.1 | |
| XM_005269564.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269621.1 | |
| XM_005269567.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269624.1 | |
| XM_005269568.4 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269625.1 | |
| XM_005269569.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269626.1 | |
| XM_005269571.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269628.1 | |
| XM_005269572.3 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_005269629.1 | |
| XM_006717642.2 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_006717705.1 | |
| XM_011539349.2 | 3373 | Missense Mutation | CCA,TCA | P,S 457 | XP_011537651.1 | |
| XM_011539351.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_011537653.1 | |
| XM_011539353.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_011537655.1 | |
| XM_011539354.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_011537656.1 | |
| XM_011539355.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_011537657.1 | |
| XM_011539357.1 | 3373 | Missense Mutation | CCA,TCA | P,S 364 | XP_011537659.1 | |
| XM_011539358.1 | 3373 | Missense Mutation | CCA,TCA | P,S 364 | XP_011537660.1 | |
| XM_017015756.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_016871245.1 | |
| XM_017015757.1 | 3373 | Missense Mutation | CCA,TCA | P,S 389 | XP_016871246.1 | |
| ZRANB1 - zinc finger RANBP2-type containing 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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