Variant #0000996427 (NC_000007.13:g.21940868C>T, NM_001277115.1:c.13547C>T (DNAH11))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21940868C>T
DNA change (hg38) -
Published as DNAH11(NM_001277115.1):c.13547C>T (p.A4516V, p.(Ala4516Val))
ISCN -
DB-ID CDCA7L_000007 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) 0.00687 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 2024-08-28 13:16:32 +02:00 (CEST)
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.13547C>T r.(?) p.(Ala4516Val)
CDCA7L NM_018719.4 -?/. - c.*1072G>A r.(=) p.(=)


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