Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1314562699
- Species
- Homo sapiens
- Symbol
- rs1314562699
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MRM1
- Location
- 17:36607690
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:36607690G>T
- HGVS.c name
- ENSEMBL:ENST00000612760.1:c.72G>T
- ENSEMBL:ENST00000614766.5:c.657G>T
- HGVS.p name
- ENSP00000481559:p.Trp219Cys
- ENSP00000482526:p.Trp24Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:36601583...36634698 (33.12 kb)
- Assembly version
- Not Available
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