Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142281097
- Species
- Homo sapiens
- Symbol
- rs142281097
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SCYL2
- Location
- 12:100339129
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000012.12:g.100339129A>G
- HGVS.c name
- ENSEMBL:ENST00000360820.7:c.2747A>G
- ENSEMBL:ENST00000635101.1:c.2759A>G
- HGVS.p name
- ENSP00000354061:p.Asn916Ser
- ENSP00000489123:p.Asn920Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:100267140...100341715 (74.58 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction