Variant #0000258660 (NC_000011.9:g.61725751_61725753del, NM_004183.3:c.848_850del (BEST1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.61725751_61725753del
DNA change (hg38) g.61958279_61958281del
Published as BEST1(NM_001139443.2):c.668_670delTCT (p.F223del)
ISCN -
DB-ID BEST1_000053 See all 6 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTH1 NM_002032.2 +/. - c.*6453_*6455del r.(=) p.(=)
BEST1 NM_004183.3 +/. - c.848_850del r.(?) p.(Phe283del)


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