Variant #0000949728 (NC_000011.9:g.61730439C>A, NC_000011.9(NM_004183.3):c.1739+74C>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.61730439C>A
DNA change (hg38) -
Published as BEST1(NM_001363593.2):c.841C>A (p.P281T)
ISCN -
DB-ID BEST1_000485
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) 0.00191 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 2023-11-27 17:35:39 +01:00 (CET)
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.*1760G>T r.(=) p.(=)
BEST1 NM_004183.3 -?/. - c.1739+74C>A r.(=) p.(=)


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