Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142398173
- Species
- Homo sapiens
- Symbol
- rs142398173
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SRSF3
- Location
- 6:36598910
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.36598910C>T
- HGVS.c name
- ENSEMBL:ENST00000339436.11:n.384C>T
- ENSEMBL:ENST00000373715.11:c.268C>T
- HGVS.p name
- ENSP00000362820:p.Arg90Cys
- ENSP00000482833:p.Arg90Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:36594353...36605911 (11.56 kb)
- Assembly version
- Not Available
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