Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs746159728
- Species
- Homo sapiens
- Symbol
- rs746159728
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRSAM1
- Location
- 9:127462362
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- (GRCh38)9:127462362C>T
- HGVS.c name
- ENSEMBL:ENST00000300417.11:c.517C>T
- ENSEMBL:ENST00000323301.8:c.517C>T
- HGVS.p name
- ENSP00000300417:p.Arg173Ter
- ENSP00000322937:p.Arg173Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:127451486...127503501 (52.02 kb)
- Assembly version
- Not Available
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