Variant #0000505684 (NC_000001.10:g.225586807G>A, NM_002296.3:c.*4198C>T (LBR))

Chromosome 1
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.225586807G>A
DNA change (hg38) g.225399105G>A
Published as DNAH14(NM_001373.1):c.13384G>A (p.(Ala4462Thr))
ISCN -
DB-ID DNAH14_000011
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) 0.00217 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH14 NM_001145154.1 -?/. - c.*375236G>A r.(=) p.(=)
DNAH14 NM_001373.1 -?/. - c.13384G>A r.(?) p.(Ala4462Thr)
LBR NM_002296.3 -?/. - c.*4198C>T r.(=) p.(=)


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