Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1419008718
- Species
- Homo sapiens
- Symbol
- rs1419008718
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLCL1
- Location
- 2:198085547
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.198085547T>G
- HGVS.c name
- ENSEMBL:ENST00000428675.6:c.2030T>G
- ENSEMBL:ENST00000435320.1:n.2485T>G
- HGVS.p name
- ENSP00000402861:p.Met677Arg
- ENSP00000414138:p.Met600Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:197804593...198572581 (767.99 kb)
- Assembly version
- Not Available
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