Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs79734099
- Species
- Homo sapiens
- Symbol
- rs79734099
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LACC1
- Location
- 13:43888867
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)13:43888867C>T
- HGVS.c name
- ENSEMBL:ENST00000325686.7:c.1018C>T
- ENSEMBL:ENST00000441843.5:c.1018C>T
- HGVS.p name
- ENSP00000317619:p.Pro340Ser
- ENSP00000391747:p.Pro340Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:43879178...43893932 (14.75 kb)
- Assembly version
- Not Available
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