Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs141695559
- Species
- Homo sapiens
- Symbol
- rs141695559
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KL
- Location
- 13:33061136
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000013.11:g.33061136C>T
- HGVS.c name
- ENSEMBL:ENST00000380099.4:c.2057C>T
- ENSEMBL:ENST00000487852.1:n.2115C>T
- HGVS.p name
- ENSP00000369442:p.Thr686Met
- NP_004786:p.Thr686Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:33016243...33066143 (49.90 kb)
- Assembly version
- Not Available
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