Variant #0000275196 (NC_000007.13:g.21934389G>A, NM_001277115.1:c.12899G>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.21934389G>A
DNA change (hg38) g.21894771G>A
Published as DNAH11(NM_001277115.1):c.12899G>A (p.R4300H)
ISCN -
DB-ID DNAH11_000125
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) 0.00049 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 2020-03-23 16:13:27 +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.12899G>A r.(?) p.(Arg4300His)
CDCA7L NM_018719.4 -?/. - c.*7551C>T r.(=) p.(=)


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