Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs763730162
- Species
- Homo sapiens
- Symbol
- rs763730162
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRC39
- Location
- 1:100160498
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:100160498C>T
- HGVS.c name
- ENSEMBL:ENST00000342895.8:c.187G>A
- ENSEMBL:ENST00000370137.6:c.187G>A
- HGVS.p name
- ENSP00000344470:p.Val63Ile
- ENSP00000359156:p.Val63Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:100148448...100179667 (31.22 kb)
- Assembly version
- Not Available
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