Variant #0001015471 (NC_000017.10:g.11502123del, NM_001372.3:c.308del (DNAH9))

Chromosome 17
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.11502123del
DNA change (hg38) -
Published as DNAH9(NM_001372.4):c.308del (p.(Phe103SerfsTer31)), DNAH9(NM_001372.4):c.308delT (p.F103Sfs*31)
ISCN -
DB-ID DNAH9_000108 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH9 NM_001372.3 +?/. - c.308del r.(?) p.(Phe103Serfs*31)


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