Variant #0000607512 (NC_000002.11:g.220149627G>A, NC_000002.11(NM_001039550.1):c.823+70G>A (DNAJB2))

Chromosome 2
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.220149627G>A
DNA change (hg38) g.219284905G>A
Published as DNAJB2(NM_006736.6):c.893G>A (p.G298E)
ISCN -
DB-ID DNAJB2_000011
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) 6.0E-5 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJB2 NM_001039550.1 ?/. - c.823+70G>A r.(=) p.(=)
PTPRN NM_001199763.1 ?/. - c.*5321C>T r.(=) p.(=)


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