Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs572457198
- Species
- Homo sapiens
- Symbol
- rs572457198
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRAT
- Location
- 4:154744737
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000004.12:g.154744737C>G
- HGVS.c name
- ENSEMBL:ENST00000336356.4:c.411C>G
- ENSEMBL:ENST00000499392.1:n.472-3452C>G
- HGVS.p name
- ENSP00000337224:p.Leu137=
- ENSP00000426761:p.Leu137=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:154626945...154753120 (126.18 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction