Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs35502907
- Species
- Homo sapiens
- Symbol
- rs35502907
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EXOSC7
- Location
- 3:45007541
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)3:45007541G>C
- HGVS.c name
- ENSEMBL:ENST00000265564.8:c.737G>C
- ENSEMBL:ENST00000461361.5:n.916G>C
- HGVS.p name
- ENSP00000265564:p.Ser246Thr
- NP_055819:p.Ser246Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:44975241...45036066 (60.83 kb)
- Assembly version
- Not Available
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