Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1192379651
- Species
- Homo sapiens
- Symbol
- rs1192379651
- Category
- Variant
- Variant type
- SNP
- Overlaps
- C1QL4
- Location
- 12:49336374
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:49336374T>C
- HGVS.c name
- ENSEMBL:ENST00000334221.5:c.104A>G
- HGVS.p name
- ENSP00000335285:p.His35Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:49332409...49337188 (4.78 kb)
- Assembly version
- Not Available
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