Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371284820
- Species
- Homo sapiens
- Symbol
- rs371284820
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMP21
- Location
- 10:125767569
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)10:125767569C>T
- HGVS.c name
- ENSEMBL:ENST00000368808.3:c.1373G>A
- ENSEMBL:ENST00000651834.1:n.575G>A
- HGVS.p name
- ENSP00000357798:p.Arg458Gln
- ENSP00000499059:p.Pro214=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:125753580...125775821 (22.24 kb)
- Assembly version
- Not Available
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