Variant #0000557165 (NC_000016.9:g.21156704G>A, NM_017539.1:c.246C>T (DNAH3))

Chromosome 16
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.21156704G>A
DNA change (hg38) g.21145383G>A
Published as DNAH3(NM_017539.2):c.246C>T (p.Y82=)
ISCN -
DB-ID DNAH3_000022
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-09 14:07:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH3 NM_017539.1 -?/. - c.246C>T r.(?) p.(Tyr82=)
TMEM159 NM_020422.4 -?/. - c.-13569G>A r.(?) p.(=)


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