Variant #0000929070 (NC_000005.9:g.34930033T>G, NC_000005.9(NM_194283.3):c.97+12T>G (DNAJC21))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34930033T>G
DNA change (hg38) -
Published as DNAJC21(NM_001012339.3):c.97+12T>G
ISCN -
DB-ID BRIX1_000002
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) 0.00105 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRIX1 NM_018321.3 -/. - c.*4433T>G r.(=) p.(=)
DNAJC21 NM_194283.3 -/. - c.97+12T>G r.(=) p.(=)


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