Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs368640893
- Species
- Homo sapiens
- Symbol
- rs368640893
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PARP3
- Location
- 3:51945583
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:51945583G>A
- HGVS.c name
- ENSEMBL:ENST00000398755.8:c.950G>A
- ENSEMBL:ENST00000417220.6:c.950G>A
- HGVS.p name
- ENSP00000381740:p.Arg317Gln
- ENSP00000395951:p.Arg317Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:51942345...51948867 (6.52 kb)
- Assembly version
- Not Available
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