Variant #0000005686 (NC_000017.11:g.43082453A>G, BRCA1(NM_007294.3):c.4308T>C)

Individual ID 00000789
Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.43082453A>G
Reference -
DB-ID BRCA1_000008 See all 287 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florencia Petracchi-CEMIC
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
Options




Variant on transcripts

Error: Query (Logged)
/variants/0000005686 returned error in code block Genome_Variant::viewEntry().
Query : SELECT vot.*, t.geneid, t.id_ncbi, e.name AS effect, ds.name AS status FROM lovd_variants_on_transcripts AS vot INNER JOIN lovd_variants AS vog ON (vot.id = vog.id) LEFT OUTER JOIN lovd_variant_effect AS e ON (vot.effectid = e.id) LEFT OUTER JOIN lovd_data_status AS ds ON (vog.statusid = ds.id) LEFT OUTER JOIN lovd_transcripts AS t ON (t.id = vot.transcriptid) WHERE (vog.statusid >= 7) AND (vot.id LIKE ?) ORDER BY t.id_ncbi ASC
Error : Error in PDOStatement::execute() while executing prepared query: SQLSTATE[HY000]: General error: 1030 Got error 28 from storage engine

  Powered by LOVD v.3.0 Build 29
LOVD software ©2004-2023 Leiden University Medical Center 		There is an LOVD update available.