Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs760056625
- Species
- Homo sapiens
- Symbol
- rs760056625
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRMT9
- Location
- 4:147673677
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.147673677T>C
- HGVS.c name
- ENSEMBL:ENST00000322396.7:c.536A>G
- ENSEMBL:ENST00000514886.1:n.525A>G
- HGVS.p name
- ENSP00000314396:p.Lys179Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:147637785...147684163 (46.38 kb)
- Assembly version
- Not Available
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