Variant #0000515833 (NC_000002.11:g.44047141dup, NM_022436.2:c.1563dup (ABCG5))

Chromosome 2
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.44047141dup
DNA change (hg38) g.43820002dup
Published as ABCG5(NM_022436.3):c.1563dupT (p.G522Wfs*39), DYNC2LI1(NM_001348913.2):c.*16-7384dupA
ISCN -
DB-ID ABCG5_000059
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC2LI1 NM_016008.3 +/. - c.*10235dup r.(?) p.(=)
ABCG5 NM_022436.2 +/. - c.1563dup r.(?) p.(Gly522TrpfsTer39)


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