Variant #0000689975 (NC_000007.13:g.21939618C>T, NM_001277115.1:c.13183C>T (DNAH11))

Chromosome 7
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.21939618C>T
DNA change (hg38) -
Published as DNAH11(NM_001277115.1):c.13183C>T (p.R4395*), DNAH11(NM_001277115.2):c.13183C>T (p.(Arg4395*))
ISCN -
DB-ID CDCA7L_000099 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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     
DNAH11 NM_001277115.1 +/. - c.13183C>T r.(?) p.(Arg4395Ter)
CDCA7L NM_018719.4 +/. - c.*2322G>A r.(=) p.(=)


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