Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs267603735
- Species
- Homo sapiens
- Symbol
- rs267603735
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SCYL2
- Location
- 12:100338703
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:100338703A>T
- HGVS.c name
- ENSEMBL:ENST00000360820.7:c.2321A>T
- ENSEMBL:ENST00000635101.1:c.2333A>T
- HGVS.p name
- ENSP00000354061:p.Asn774Ile
- ENSP00000489123:p.Asn778Ile
- 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
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