Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1168933295
- Species
- Homo sapiens
- Symbol
- rs1168933295
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUBPL
- Location
- 14:31599305
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- (GRCh38)14:31599305T>A
- HGVS.c name
- ENSEMBL:ENST00000281081.12:c.308T>A
- ENSEMBL:ENST00000547839.5:n.350T>A
- HGVS.p name
- ENSP00000281081:p.Leu103Ter
- ENSP00000447234:p.Leu51Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:31489956...31861224 (371.27 kb)
- Assembly version
- Not Available
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