Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs150076465
- Species
- Homo sapiens
- Symbol
- rs150076465
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FRMD4A
- Location
- 10:13810915
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000010.11:g.13810915G>A
- HGVS.c name
- ENSEMBL:ENST00000264546.10:c.211-7C>T
- ENSEMBL:ENST00000342409.3:n.541-7C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:13643706...14462142 (818.44 kb)
- Assembly version
- Not Available
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