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- SNP ID:
- rs760163335
- Gene
-
ZNF226 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 44176015 - 44176015 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
GCATGATTCACACAGGACAGAAATC[G/A]TACCAGTGTAATGAGTGTAAAAAAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
ZNF226 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 |
| ZNF226 - zinc finger protein 226 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001032372.1 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | NP_001027544.1 | |
| NM_001032373.1 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | NP_001027545.1 | |
| NM_001032374.1 | 1572 | Intron | NP_001027546.1 | |||
| NM_001146220.2 | 1572 | Intron | NP_001139692.1 | |||
| NM_001319088.1 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | NP_001306017.1 | |
| NM_001319089.1 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | NP_001306018.1 | |
| NM_001319090.1 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | NP_001306019.1 | |
| NM_015919.3 | 1572 | Intron | NP_057003.2 | |||
| NM_016444.2 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | NP_057528.2 | |
| XM_005259227.2 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | XP_005259284.1 | |
| XM_006723367.3 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | XP_006723430.1 | |
| XM_006723368.3 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | XP_006723431.1 | |
| XM_006723369.2 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | XP_006723432.1 | |
| XM_017027262.1 | 1572 | Silent Mutation | TCA,TCG | S,S 251 | XP_016882751.1 | |
| XM_017027263.1 | 1572 | Silent Mutation | TCA,TCG | S,S 134 | XP_016882752.1 | |
| XM_017027264.1 | 1572 | Silent Mutation | TCA,TCG | S,S 134 | XP_016882753.1 | |
| XM_017027265.1 | 1572 | Intron | XP_016882754.1 | |||
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