Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142208662
- Species
- Homo sapiens
- Symbol
- rs142208662
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLEKHG4B
- Location
- 5:143375
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000005.10:g.143375C>T
- HGVS.c name
- ENSEMBL:ENST00000283426.11:c.620-5C>T
- ENSEMBL:ENST00000502646.1:c.362-5C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:92168...189972 (97.80 kb)
- Assembly version
- Not Available
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