Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs397508057
- Species
- Homo sapiens
- Symbol
- rs397508057
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BRCA2
- Location
- 13:32319103
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)13:32319103T>C
- HGVS.c name
- ENSEMBL:ENST00000470094.2:n.293T>C
- ENSEMBL:ENST00000530893.7:c.-276T>C
- HGVS.p name
- ENSP00000439902:p.Phe32Leu
- ENSP00000505508:p.Phe32Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:32315077...32400268 (85.19 kb)
- Assembly version
- Not Available
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