Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs141025723
- Species
- Homo sapiens
- Symbol
- rs141025723
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DGCR6L
- Location
- 22:20315469
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)22:20315469T>C
- HGVS.c name
- ENSEMBL:ENST00000248879.8:c.380A>G
- ENSEMBL:ENST00000405465.3:c.266A>G
- HGVS.p name
- ENSP00000248879:p.Glu127Gly
- ENSP00000386052:p.Glu89Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:20314238...20320080 (5.84 kb)
- Assembly version
- Not Available
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