Variant #0000654851 (NC_000003.11:g.180705961C>A, NC_000003.11(NM_145261.3):c.55+5G>T (DNAJC19))

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.180705961C>A
DNA change (hg38) g.180988173C>A
Published as DNAJC19(NM_145261.4):c.55+5G>T
ISCN -
DB-ID DNAJC19_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJC19 NM_145261.3 ?/. - c.55+5G>T r.spl? p.?


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