Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1226010589
- Species
- Homo sapiens
- Symbol
- rs1226010589
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MAP3K10
- Location
- 19:40213996
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:40213996G>A
- HGVS.c name
- ENSEMBL:ENST00000253055.8:c.2317G>A
- ENSEMBL:ENST00000597986.5:n.1320G>A
- HGVS.p name
- ENSP00000253055:p.Ala773Thr
- XP_011525284:p.Ala781Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:40191426...40215575 (24.15 kb)
- Assembly version
- Not Available
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