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- SNP ID:
- rs145687726
- Gene
-
HCG16ZNF311 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.6: 28995693 - 28995693 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
CACCCATAGTGTTTCTCCCGAGTAT[G/T]GATTCGTTTGTGTTTGCTTAGGTCT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
HCG16 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 |
| HCG16 - HLA complex group 16 (non-protein coding) | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| ZNF311 - zinc finger protein 311 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001010877.3 | 1772 | Missense Mutation | AAT,CAT | N,H 437 | NP_001010877.2 | |
| NM_001318534.1 | 1772 | Missense Mutation | AAT,CAT | N,H 345 | NP_001305463.1 | |
| NM_001318535.1 | 1772 | Missense Mutation | AAT,CAT | N,H 345 | NP_001305464.1 | |
| XM_005249019.3 | 1772 | Missense Mutation | AAT,CAT | N,H 470 | XP_005249076.1 | |
| XM_006715067.2 | 1772 | Missense Mutation | AAT,CAT | N,H 470 | XP_006715130.1 | |
| XM_011514510.1 | 1772 | Missense Mutation | AAT,CAT | N,H 470 | XP_011512812.1 | |
| XM_011514511.2 | 1772 | Missense Mutation | AAT,CAT | N,H 470 | XP_011512813.1 | |
| XM_011514512.1 | 1772 | Missense Mutation | AAT,CAT | N,H 462 | XP_011512814.1 | |
| XM_011514513.1 | 1772 | Missense Mutation | AAT,CAT | N,H 461 | XP_011512815.1 | |
| XM_011514514.1 | 1772 | Missense Mutation | AAT,CAT | N,H 445 | XP_011512816.1 | |
| XM_011514516.1 | 1772 | Missense Mutation | AAT,CAT | N,H 389 | XP_011512818.1 | |
| XM_011514517.1 | 1772 | Missense Mutation | AAT,CAT | N,H 345 | XP_011512819.1 | |
| XM_011514518.1 | 1772 | Missense Mutation | AAT,CAT | N,H 345 | XP_011512820.1 | |
| XM_017010756.1 | 1772 | Missense Mutation | AAT,CAT | N,H 470 | XP_016866245.1 | |
| XM_017010757.1 | 1772 | Missense Mutation | AAT,CAT | N,H 470 | XP_016866246.1 | |
| XM_017010758.1 | 1772 | Missense Mutation | AAT,CAT | N,H 437 | XP_016866247.1 | |
| XM_017010759.1 | 1772 | Missense Mutation | AAT,CAT | N,H 437 | XP_016866248.1 | |
| XM_017010760.1 | 1772 | Missense Mutation | AAT,CAT | N,H 389 | XP_016866249.1 | |
| XM_017010761.1 | 1772 | Missense Mutation | AAT,CAT | N,H 345 | XP_016866250.1 | |
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