Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371981770
- Species
- Homo sapiens
- Symbol
- rs371981770
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FRMD4A
- Location
- 10:13670453
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)10:13670453C>T
- HGVS.c name
- ENSEMBL:ENST00000264546.10:c.1426G>A
- ENSEMBL:ENST00000357447.7:c.1327G>A
- HGVS.p name
- ENSP00000264546:p.Gly476Arg
- ENSP00000350032:p.Gly443Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:13643706...14462142 (818.44 kb)
- Assembly version
- Not Available
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