Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs148377517
- Species
- Homo sapiens
- Symbol
- rs148377517
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FITM2
- Location
- 20:44311053
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000020.11:g.44311053C>T
- HGVS.c name
- ENSEMBL:ENST00000396825.4:c.96G>A
- RefSeq:NM_001080472.4:c.96G>A
- HGVS.p name
- ENSP00000380037:p.Met32Ile
- NP_001073941:p.Met32Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:44302840...44311202 (8.36 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction