Variant #0000544712 (NC_000011.9:g.61730295G>A, NM_004183.3:c.1669G>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.61730295G>A
DNA change (hg38) g.61962823G>A
Published as BEST1(NM_001139443.2):c.1489G>A (p.E497K), BEST1(NM_004183.3):c.1669G>A (p.E557K)
ISCN -
DB-ID BEST1_000061 See all 4 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) 0.00046 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.*1904C>T r.(=) p.(=)
BEST1 NM_004183.3 -?/. - c.1669G>A r.(?) p.(Glu557Lys)


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