Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs183705571
- Species
- Homo sapiens
- Symbol
- rs183705571
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EXOSC5
- Location
- 19:41397210
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:41397210C>G
- HGVS.c name
- ENSEMBL:ENST00000221233.9:c.119G>C
- ENSEMBL:ENST00000593523.2:n.153G>C
- HGVS.p name
- ENSP00000221233:p.Arg40Pro
- ENSP00000471002:p.Arg40Pro
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:41386371...41397362 (10.99 kb)
- Assembly version
- Not Available
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