Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1775596990
- Species
- Homo sapiens
- Symbol
- rs1775596990
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PERP
- Location
- 6:138092172
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- NC_000006.12:g.138092172C>T
- HGVS.c name
- ENSEMBL:ENST00000421351.4:c.452G>A
- RefSeq:NM_022121.5:c.452G>A
- HGVS.p name
- ENSP00000397157:p.Trp151Ter
- NP_071404:p.Trp151Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:138088505...138107419 (18.91 kb)
- Assembly version
- Not Available
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