Variant #0001052629 (NC_000007.13:g.21882155C>T, NC_000007.13(NM_001277115.1):c.10692-7C>T (DNAH11))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21882155C>T
DNA change (hg38) -
Published as DNAH11(NM_001277115.1):c.10692-7C>T, DNAH11(NM_001277115.2):c.10692-7C>T
ISCN -
DB-ID DNAH11_000103 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) 0.00025 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH11 NM_001277115.1 ?/. - c.10692-7C>T r.(=) p.(=)
CDCA7L NM_018719.4 ?/. - c.*59785G>A r.(=) p.(=)


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