Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1450402393
- Species
- Homo sapiens
- Symbol
- rs1450402393
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARMC8
- Location
- 3:138245175
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:138245175C>T
- HGVS.c name
- ENSEMBL:ENST00000358441.6:c.1084C>T
- ENSEMBL:ENST00000460495.5:n.644C>T
- HGVS.p name
- ENSP00000351221:p.Arg362Trp
- ENSP00000417049:p.Arg303Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:138187248...138298389 (111.14 kb)
- Assembly version
- Not Available
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