Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs865838543
- Species
- Homo sapiens
- Symbol
- rs865838543
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDH1
- Location
- 16:68738314
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- (GRCh38)16:68738314C>A
- HGVS.c name
- ENSEMBL:ENST00000261769.10:c.66C>A
- ENSEMBL:ENST00000422392.6:c.66C>A
- HGVS.p name
- ENSP00000261769:p.Cys22Ter
- ENSP00000414946:p.Cys22Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:68737292...68835537 (98.25 kb)
- Assembly version
- Not Available
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