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- SNP ID:
- rs782585756
- Gene
-
ZNF518A - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.10: 96157493 - 96157493 on Build GRCh38
- Polymorphism:
- G/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TGATAAAGCCCCTGAATCAGAGTCA[G/C]AGAAGCCAACTCCTCTGTCCACTGG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF518A 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 |
| ZNF518A - zinc finger protein 518A | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001278524.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | NP_001265453.1 | |
| NM_001278525.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | NP_001265454.1 | |
| NM_001278526.1 | 1887 | Intron | NP_001265455.1 | |||
| NM_014803.3 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | NP_055618.2 | |
| XM_011540406.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538708.1 | |
| XM_011540408.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538710.1 | |
| XM_011540410.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538712.1 | |
| XM_011540412.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538714.1 | |
| XM_011540413.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538715.1 | |
| XM_011540415.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538717.1 | |
| XM_011540418.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538720.1 | |
| XM_011540419.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538721.1 | |
| XM_011540420.2 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_011538722.1 | |
| XM_017016986.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872475.1 | |
| XM_017016987.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872476.1 | |
| XM_017016988.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872477.1 | |
| XM_017016989.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872478.1 | |
| XM_017016990.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872479.1 | |
| XM_017016991.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872480.1 | |
| XM_017016992.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872481.1 | |
| XM_017016993.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872482.1 | |
| XM_017016994.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872483.1 | |
| XM_017016995.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872484.1 | |
| XM_017016996.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872485.1 | |
| XM_017016997.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872486.1 | |
| XM_017016998.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872487.1 | |
| XM_017016999.1 | 1887 | Missense Mutation | CAG,GAG | Q,E 391 | XP_016872488.1 | |
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