Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778872333
- Species
- Homo sapiens
- Symbol
- rs778872333
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRMT9
- Location
- 4:147642866
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)4:147642866G>A
- HGVS.c name
- ENSEMBL:ENST00000322396.7:c.2120C>T
- ENSEMBL:ENST00000508208.5:c.779+11361G>A
- HGVS.p name
- ENSP00000314396:p.Thr707Ile
- XP_047272349:p.Thr402Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:147637785...147684163 (46.38 kb)
- Assembly version
- Not Available
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