Variant #0000261965 (NC_000001.10:g.150530513dup, NM_019032.4:c.2270dup (ADAMTSL4))

Chromosome 1
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.150530513dup
DNA change (hg38) g.150558037dup
Published as ADAMTSL4(NM_001288608.1):c.2339dupG (p.G781Wfs*59), ADAMTSL4(NM_019032.5):c.2270dupG (p.G758Wfs*59)
ISCN -
DB-ID ADAMTSL4_000037 See all 7 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTSL4 NM_019032.4 +/. - c.2270dup r.(?) p.(Gly758TrpfsTer59)


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