Variant #0000331484 (NC_000007.13:g.21940816G>A, NM_001277115.1:c.13495G>A (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.21940816G>A
DNA change (hg38) g.21901198G>A
Published as DNAH11(NM_001277115.1):c.13495G>A (p.E4499K, p.(Glu4499Lys))
ISCN -
DB-ID CDCA7L_000005 See all 3 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) 0.00465 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.13495G>A r.(?) p.(Glu4499Lys)
CDCA7L NM_018719.4 -?/. - c.*1124C>T r.(=) p.(=)


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