Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199775360
- Species
- Homo sapiens
- Symbol
- rs199775360
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IQCB1
- Location
- 3:121770403
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:121770403T>G
- HGVS.c name
- ENSEMBL:ENST00000310864.11:c.1739A>C
- ENSEMBL:ENST00000349820.10:c.1340A>C
- HGVS.p name
- ENSP00000311505:p.Lys580Thr
- ENSP00000323756:p.Lys447Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:121769761...121835079 (65.32 kb)
- Assembly version
- Not Available
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