Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1782913333
- Species
- Homo sapiens
- Symbol
- rs1782913333
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CPVL
- Location
- 7:29064135
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.29064135C>G
- HGVS.c name
- ENSEMBL:ENST00000265394.10:c.1063G>C
- ENSEMBL:ENST00000396276.7:c.1063G>C
- HGVS.p name
- ENSP00000265394:p.Val355Leu
- ENSP00000379572:p.Val355Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:28994636...29195451 (200.82 kb)
- Assembly version
- Not Available
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