Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs193920789
- Species
- Homo sapiens
- Symbol
- rs193920789
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TP53
- Location
- 17:7674249
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- (GRCh38)17:7674249A>T
- HGVS.c name
- ENSEMBL:ENST00000359597.8:c.714T>A
- ENSEMBL:ENST00000413465.6:c.714T>A
- HGVS.p name
- ENSP00000352610:p.Cys238Ter
- ENSP00000410739:p.Cys238Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:7661779...7687546 (25.77 kb)
- Assembly version
- Not Available
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