Variant #0000520334 (NC_000003.11:g.52430486G>A, NM_015512.4:c.11362G>A (DNAH1))

Chromosome 3
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.52430486G>A
DNA change (hg38) g.52396470G>A
Published as DNAH1(NM_015512.4):c.11362G>A (p.(Gly3788Ser))
ISCN -
DB-ID DNAH1_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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 ?/. - c.*5818C>T r.(=) p.(=)
DNAH1 NM_015512.4 ?/. - c.11362G>A r.(?) p.(Gly3788Ser)


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