Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs868708982
- Species
- Homo sapiens
- Symbol
- rs868708982
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLEKHM3
- Location
- 2:207977062
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:207977062C>T
- HGVS.c name
- ENSEMBL:ENST00000427836.8:c.1135G>A
- ENSEMBL:ENST00000447645.5:c.389G>A
- HGVS.p name
- ENSP00000395354:p.Gly130Asp
- ENSP00000400150:p.Ala379Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:207821288...208025527 (204.24 kb)
- Assembly version
- Not Available
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