Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs377504175
- Species
- Homo sapiens
- Symbol
- rs377504175
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ARHGEF33
- Location
- 2:38937386
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:38937386C>T
- HGVS.c name
- ENSEMBL:ENST00000398800.8:c.617C>T
- HGVS.p name
- ENSP00000381780:p.Ser206Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:38889875...38975454 (85.58 kb)
- Assembly version
- Not Available
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