Variant #0000531700 (NC_000007.13:g.21940694C>T, NM_001277115.1:c.13373C>T (DNAH11))

Chromosome 7
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.21940694C>T
DNA change (hg38) g.21901076C>T
Published as DNAH11(NM_001277115.1):c.13373C>T (p.P4458L), DNAH11(NM_001277115.2):c.13373C>T (p.P4458L)
ISCN -
DB-ID CDCA7L_000002 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) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH11 NM_001277115.1 +?/. - c.13373C>T r.(?) p.(Pro4458Leu)
CDCA7L NM_018719.4 +?/. - c.*1246G>A r.(=) p.(=)


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