Variant #0000544819 (NC_000011.9:g.64004692C>T, NM_005528.3:c.*3036C>T (DNAJC4))

Chromosome 11
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.64004692C>T
DNA change (hg38) g.64237220C>T
Published as VEGFB(NM_001243733.1):c.408C>T (p.(=))
ISCN -
DB-ID DNAJC4_000005
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) 0.23276 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 17:23:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VEGFB NM_003377.4 -?/. - c.408C>T r.(?) p.(Asp136=)
FKBP2 NM_004470.3 -?/. - c.-3917C>T r.(?) p.(=)
DNAJC4 NM_005528.3 -?/. - c.*3036C>T r.(=) p.(=)


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