Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs148834205
- Species
- Homo sapiens
- Symbol
- rs148834205
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DNAAF19
- Location
- 17:44902561
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:44902561C>T
- HGVS.c name
- ENSEMBL:ENST00000357776.6:c.473C>T
- ENSEMBL:ENST00000410006.6:c.473C>T
- HGVS.p name
- ENSP00000350420:p.Ala158Val
- ENSP00000387252:p.Ala158Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:44899142...44905390 (6.25 kb)
- Assembly version
- Not Available
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