Variant #0000805224 (NC_000011.9:g.61724901T>A, NM_004183.3:c.679T>A (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.61724901T>A
DNA change (hg38) -
Published as BEST1(NM_001139443.2):c.499T>A (p.Y167N), BEST1(NM_004183.3):c.679T>A (p.Y227N), BEST1(NM_004183.4):c.679T>A (p.(Tyr227Asn))
ISCN -
DB-ID BEST1_000022 See all 22 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.*7298A>T r.(=) p.(=)
BEST1 NM_004183.3 +/. - c.679T>A r.(?) p.(Tyr227Asn)


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