Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs764819983
- Species
- Homo sapiens
- Symbol
- rs764819983
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PHF1
- Location
- 6:33415017
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.33415017C>T
- HGVS.c name
- ENSEMBL:ENST00000374512.7:c.1101C>T
- ENSEMBL:ENST00000374516.8:c.1112C>T
- HGVS.p name
- ENSP00000363636:p.Ala367=
- ENSP00000363640:p.Pro371Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:33410399...33416453 (6.05 kb)
- Assembly version
- Not Available
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