Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142086610
- Species
- Homo sapiens
- Symbol
- rs142086610
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRMT9
- Location
- 4:147638651
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)4:147638651A>T
- HGVS.c name
- ENSEMBL:ENST00000322396.7:c.2419T>A
- ENSEMBL:ENST00000508208.5:c.779+7146A>T
- HGVS.p name
- ENSP00000314396:p.Ser807Thr
- XP_047272349:p.Ser502Thr
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction