Variant #0000275274 (NC_000016.9:g.20996874_20996876del, NM_017539.1:c.7193_7195del (DNAH3))

Chromosome 16
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.20996874_20996876del
DNA change (hg38) g.20985552_20985554del
Published as DNAH3(NM_017539.2):c.7193_7195delACA (p.N2398del)
ISCN -
DB-ID DNAH3_000004
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) Retrieve
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     
DNAH3 NM_017539.1 ?/. - c.7193_7195del r.(?) p.(Asn2398del)
TMEM159 NM_020422.4 ?/. - c.-173399_-173397del r.(?) p.(=)


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