Variant #0000267460 (NC_000005.9:g.13902220T>C, NM_001369.2:c.1672A>G (DNAH5))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13902220T>C
DNA change (hg38) g.13902111T>C
Published as DNAH5(NM_001369.2):c.1672A>G (p.T558A), DNAH5(NM_001369.3):c.1672A>G (p.T558A)
ISCN -
DB-ID DNAH5_000103 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) 0.39702 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
DNAH5 NM_001369.2 -/. - c.1672A>G r.(?) p.(Thr558Ala)


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