Variant #0000525556 (NC_000005.9:g.34950282A>G, NM_194283.3:c.1328A>G (DNAJC21))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34950282A>G
DNA change (hg38) g.34950177A>G
Published as DNAJC21(NM_194283.3):c.1328A>G (p.D443G), DNAJC21(NM_194283.4):c.1328A>G (p.D443G)
ISCN -
DB-ID DNAJC21_000002 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJC21 NM_194283.3 -?/. - c.1328A>G r.(?) p.(Asp443Gly)


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