Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1263252182
- Species
- Homo sapiens
- Symbol
- rs1263252182
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRC73
- Location
- 6:43509763
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- NC_000006.12:g.43509763A>G
- HGVS.c name
- ENSEMBL:ENST00000372441.2:c.23T>C
- ENSEMBL:ENST00000428025.6:c.-142A>G
- HGVS.p name
- ENSP00000361518:p.Ile8Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:43506968...43510346 (3.38 kb)
- Assembly version
- Not Available
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