Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142676086
- Species
- Homo sapiens
- Symbol
- rs142676086
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIAA2013
- Location
- 1:11923439
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:11923439C>T
- HGVS.c name
- ENSEMBL:ENST00000376572.8:c.1084G>A
- ENSEMBL:ENST00000376576.3:c.1084G>A
- HGVS.p name
- ENSP00000365756:p.Val362Met
- ENSP00000365760:p.Val362Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:11919591...11926428 (6.84 kb)
- Assembly version
- Not Available
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