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- SNP ID:
- rs753071531
- Gene
-
C19orf45ZNF358 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 7508294 - 7508294 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
GACGAGTTTCCTTTCAAGTACCAGG[G/A]CCCAGCAGCCCTGAGACTGAAAAAT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C19orf45 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 |
| C19orf45 - chromosome 19 open reading frame 45 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_198534.2 | 1448 | Missense Mutation | GAC,GGC | D,G 461 | NP_940936.2 | |
| XM_005272473.3 | 1448 | Missense Mutation | GAC,GGC | D,G 461 | XP_005272530.1 | |
| XM_011527993.1 | 1448 | Missense Mutation | GAC,GGC | D,G 436 | XP_011526295.1 | |
| XM_011527995.2 | 1448 | Intron | XP_011526297.1 | |||
| ZNF358 - zinc finger protein 358 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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