Variant #0000807136 (NC_000016.9:g.20975042A>C, NM_017539.1:c.10164T>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.20975042A>C
DNA change (hg38) -
Published as DNAH3(NM_001347886.1):c.10026T>G (p.I3342M)
ISCN -
DB-ID DNAH3_000033
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 2021-09-17 14:40:49 +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.10164T>G r.(?) p.(Ile3388Met)
TMEM159 NM_020422.4 ?/. - c.-195231A>C r.(?) p.(=)


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