Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1004391153
- Species
- Homo sapiens
- Symbol
- rs1004391153
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AFG2A
- Location
- 4:123314057
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:123314057C>T
- HGVS.c name
- ENSEMBL:ENST00000274008.5:c.2675C>T
- ENSEMBL:ENST00000675612.1:c.2744C>T
- HGVS.p name
- ENSP00000274008:p.Thr892Ile
- ENSP00000502453:p.Thr915Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:122923070...123319433 (396.36 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction