Variant #0000520320 (NC_000003.11:g.52387129_52387132dup, NM_015512.4:c.3038_3041dup (DNAH1))

Chromosome 3
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.52387129_52387132dup
DNA change (hg38) g.52353113_52353116dup
Published as DNAH1(NM_015512.4):c.3038_3041dupTCTC (p.R1015Lfs*19), DNAH1(NM_015512.5):c.3038_3041dupTCTC (p.R1015Lfs*19)
ISCN -
DB-ID DNAH1_000024 See all 2 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH1 NM_015512.4 +?/. - c.3038_3041dup r.(?) p.(Arg1015LeufsTer19)


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