Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs786202707
- Species
- Homo sapiens
- Symbol
- rs786202707
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BRCA2
- Location
- 13:32325140
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000013.11:g.32325140A>G
- HGVS.c name
- ENSEMBL:ENST00000470094.2:n.580A>G
- ENSEMBL:ENST00000530893.7:c.12A>G
- HGVS.p name
- ENSP00000439902:p.Ala127=
- ENSP00000499438:p.Ala4=
- 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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