Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs375946603
- Species
- Homo sapiens
- Symbol
- rs375946603
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TSEN15
- Location
- 1:184072214
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:184072214G>A
- HGVS.c name
- ENSEMBL:ENST00000361641.6:c.411G>A
- ENSEMBL:ENST00000423085.7:c.354-613G>A
- HGVS.p name
- ENSP00000355299:p.Met137Ile
- ENSP00000493902:p.Met137Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:184051651...184123978 (72.33 kb)
- Assembly version
- Not Available
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