Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200628146
- Species
- Homo sapiens
- Symbol
- rs200628146
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MYO5C
- Location
- 15:52282867
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:52282867G>A
- HGVS.c name
- ENSEMBL:ENST00000261839.12:c.53C>T
- ENSEMBL:ENST00000541028.5:n.160-3193C>T
- HGVS.p name
- ENSP00000261839:p.Pro18Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:52192322...52295804 (103.48 kb)
- Assembly version
- Not Available
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