Variant #0000018016 (NC_000005.9:g.13900321G>T, NM_001369.2:c.2253C>A (DNAH5))

Chromosome 5
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.13900321G>T
DNA change (hg38) g.13900212G>T
Published as -
ISCN -
DB-ID DNAH5_000002 See all 4 reported entries
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00988 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-08 23:53:32 +02:00 (CEST)
Date last edited 2013-05-31 18:48:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH5 NM_001369.2 ?/? ? c.2253C>A r.(?) p.(Asn751Lys)



Screenings

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