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- SNP ID:
- rs770874199
- Gene
-
MIR6784PLCD3 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.17: 45120440 - 45120440 on Build GRCh38
- Polymorphism:
- T/C, Transition substitution
- Context Sequence [VIC/FAM]:
CTGGTTGGAGTCAGCCCGGTGCAGA[T/C]AGGAGTGGATCCAGGTGTGGGTGCT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608795
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Literature Links: |
MIR6784 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 |
| MIR6784 - microRNA 6784 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| PLCD3 - phospholipase C delta 3 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_133373.4 | 692 | Missense Mutation | TAT,TGT | Y,C 190 | NP_588614.1 | |
| XM_011524253.2 | 692 | Missense Mutation | TAT,TGT | Y,C 190 | XP_011522555.1 | |
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