Variant #0000929929 (NC_000011.9:g.61724329G>A, NM_004183.3:c.495G>A (BEST1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61724329G>A
DNA change (hg38) -
Published as BEST1(NM_001139443.2):c.315G>A (p.P105=)
ISCN -
DB-ID BEST1_000481
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) 0.00061 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTH1 NM_002032.2 -?/. - c.*7870C>T r.(=) p.(=)
BEST1 NM_004183.3 -?/. - c.495G>A r.(?) p.(=)


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