Variant #0000517917 (NC_000003.11:g.132212989T>G, DNAJC13(NM_015268.3):c.3827T>G)

Chromosome 3
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.132212989T>G
DNA change (hg38) g.132494145T>G
Published as DNAJC13(NM_001329126.1):c.3842T>G (p.V1281G)
ISCN -
DB-ID DNAJC13_000047
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 View details
Owner VKGL-NL_Rotterdam
Database submission license No license selected
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJC13 NM_015268.3 ?/. - c.3827T>G r.(?) p.(Val1276Gly)