Variant #0000275400 (NC_000001.10:g.65830312_65830313del, NC_000001.10(NM_001256864.1):c.194-6_194-5del (DNAJC6))

Chromosome 1
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.65830312_65830313del
DNA change (hg38) g.65364629_65364630del
Published as DNAJC6(NM_001256864.2):c.194-6_194-5delTG
ISCN -
DB-ID DNAJC6_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-04 16:08:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJC6 NM_001256864.1 -?/. - c.194-6_194-5del r.spl? p.?


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