Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs876661106
- Species
- Homo sapiens
- Symbol
- rs876661106
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDH1
- Location
- 16:68801843
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- NC_000016.10:g.68801843A>T
- HGVS.c name
- ENSEMBL:ENST00000261769.10:c.337A>T
- ENSEMBL:ENST00000422392.6:c.337A>T
- HGVS.p name
- ENSP00000261769:p.Lys113Ter
- ENSP00000414946:p.Lys113Ter
- 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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