Variant #0000981685 (NC_000016.9:g.20970634T>C, NM_017539.1:c.10693A>G (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.20970634T>C
DNA change (hg38) -
Published as DNAH3(NM_001347886.2):c.10555A>G (p.(Met3519Val))
ISCN -
DB-ID DNAH3_000038
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH3 NM_017539.1 ?/. - c.10693A>G r.(?) p.(Met3565Val)
TMEM159 NM_020422.4 ?/. - c.-199639T>C r.(?) p.(=)


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