Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs759987328
- Species
- Homo sapiens
- Symbol
- rs759987328
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DESI2
- Location
- 1:244689300
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:244689300C>G
- HGVS.c name
- ENSEMBL:ENST00000263831.11:c.116-2584C>G
- ENSEMBL:ENST00000302550.16:c.167C>G
- HGVS.p name
- ENSP00000306528:p.Ser56Cys
- ENSP00000394555:p.Ser73Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244653103...244709033 (55.93 kb)
- Assembly version
- Not Available
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