Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778543586
- Species
- Homo sapiens
- Symbol
- rs778543586
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PPP2R1A
- Location
- 19:52222127
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:52222127T>C
- HGVS.c name
- ENSEMBL:ENST00000322088.11:c.1547T>C
- ENSEMBL:ENST00000391791.4:c.180T>C
- HGVS.p name
- ENSP00000324804:p.Ile516Thr
- ENSP00000375668:p.His60=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:52170936...52229518 (58.58 kb)
- Assembly version
- Not Available
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