Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371270716
- Species
- Homo sapiens
- Symbol
- rs371270716
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BRDT
- Location
- 1:91968164
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.91968164C>T
- HGVS.c name
- ENSEMBL:ENST00000394530.7:c.211C>T
- ENSEMBL:ENST00000399546.7:c.349C>T
- HGVS.p name
- ENSP00000378038:p.Leu71Phe
- ENSP00000384051:p.Leu117Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:91949343...92014428 (65.09 kb)
- Assembly version
- Not Available
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