Variant #0000805225 (NC_000011.9:g.61727469G>A, NM_004183.3:c.1054G>A (BEST1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.61727469G>A
DNA change (hg38) -
Published as BEST1(NM_001139443.1):c.874G>A (p.A292T), BEST1(NM_001363593.2):c.82G>A (p.A28T)
ISCN -
DB-ID BEST1_000080 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTH1 NM_002032.2 ?/. - c.*4730C>T r.(=) p.(=)
BEST1 NM_004183.3 ?/. - c.1054G>A r.(?) p.(Ala352Thr)


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