Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1479687090
- Species
- Homo sapiens
- Symbol
- rs1479687090
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GREB1L
- Location
- 18:21395403
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)18:21395403A>G
- HGVS.c name
- ENSEMBL:ENST00000269218.10:c.374A>G
- ENSEMBL:ENST00000424526.7:c.374A>G
- HGVS.p name
- ENSP00000269218:p.Lys125Arg
- ENSP00000412060:p.Lys125Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:21242232...21526112 (283.88 kb)
- Assembly version
- Not Available
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