Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200793446
- Species
- Homo sapiens
- Symbol
- rs200793446
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RTCB
- Location
- 22:32401757
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)22:32401757T>C
- HGVS.c name
- ENSEMBL:ENST00000216038.6:c.487A>G
- ENSEMBL:ENST00000476619.5:n.368A>G
- HGVS.p name
- ENSP00000216038:p.Met163Val
- NP_055121:p.Met163Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:32387582...32412248 (24.67 kb)
- Assembly version
- Not Available
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