Variant #0000723522 (NC_000011.9:g.61730285dup, NM_004183.3:c.1659dup (BEST1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.61730285dup
DNA change (hg38) -
Published as BEST1(NM_004183.3):c.1659dupA (p.E554Rfs*29)
ISCN -
DB-ID BEST1_000129
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.*1916dup r.(?) p.(=)
BEST1 NM_004183.3 +?/. - c.1659dup r.(?) p.(Glu554Argfs*29)


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