Variant #0000854750 (NC_000017.10:g.11535971T>G, NM_001372.3:c.1586T>G (DNAH9))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11535971T>G
DNA change (hg38) -
Published as DNAH9(NM_001372.3):c.1586T>G (p.I529S), DNAH9(NM_001372.4):c.1586T>G (p.I529S)
ISCN -
DB-ID DNAH9_000076 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) 0.00042 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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH9 NM_001372.3 ?/. - c.1586T>G r.(?) p.(Ile529Ser)


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