Variant #0000275204 (NC_000007.13:g.21939698G>C, NM_001277115.1:c.13263G>C (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.21939698G>C
DNA change (hg38) g.21900080G>C
Published as DNAH11(NM_001277115.1):c.13263G>C (p.P4421=)
ISCN -
DB-ID DNAH11_000134
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) 0.01111 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 15:17:31 +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.13263G>C r.(?) p.(Pro4421=)
CDCA7L NM_018719.4 -?/. - c.*2242C>G r.(=) p.(=)


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