Variant #0000514706 (NC_000002.11:g.220149542G>C, NM_001039550.1:c.808G>C (DNAJB2))

Chromosome 2
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.220149542G>C
DNA change (hg38) g.219284820G>C
Published as DNAJB2(NM_001039550.2):c.808G>C (p.G270R), DNAJB2(NM_006736.6):c.808G>C (p.G270R)
ISCN -
DB-ID DNAJB2_000008 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) 0.00264 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJB2 NM_001039550.1 -/. - c.808G>C r.(?) p.(Gly270Arg)
PTPRN NM_001199763.1 -/. - c.*5406C>G r.(=) p.(=)


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