Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142318812
- Species
- Homo sapiens
- Symbol
- rs142318812
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FITM2
- Location
- 20:44306641
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)20:44306641T>C
- HGVS.c name
- ENSEMBL:ENST00000396825.4:c.773A>G
- RefSeq:NM_001080472.4:c.773A>G
- HGVS.p name
- ENSP00000380037:p.Asp258Gly
- NP_001073941:p.Asp258Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:44302840...44311202 (8.36 kb)
- Assembly version
- Not Available
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