Variant #0000866617 (NC_000021.8:g.34860959_34860960insG, NM_001040192.1:c.741_742insC (DNAJC28))

Chromosome 21
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.34860959_34860960insG
DNA change (hg38) -
Published as DNAJC28(NM_017833.4):c.741_742insC (p.I248Hfs*3)
ISCN -
DB-ID DNAJC28_000006
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJC28 NM_001040192.1 ?/. - c.741_742insC r.(?) p.(Ile248Hisfs*3)


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