Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2150995270
- Species
- Homo sapiens
- Symbol
- rs2150995270
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TP53
- Location
- 17:7670703
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:7670703C>G
- HGVS.c name
- ENSEMBL:ENST00000359597.8:c.993+2832G>C
- ENSEMBL:ENST00000413465.6:c.782+3478G>C
- HGVS.p name
- ENSP00000424104:p.Glu336Gln
- ENSP00000426252:p.Glu336Gln
- 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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