Variant #0000249898 (NC_000001.10:g.65860687A>C, NM_001256864.1:c.2010A>C (DNAJC6))

Chromosome 1
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.65860687A>C
DNA change (hg38) g.65395004A>C
Published as DNAJC6(NM_001256864.2):c.2010A>C (p.P670=), DNAJC6(NM_014787.3):c.1839A>C (p.P613=)
ISCN -
DB-ID DNAJC6_000019 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) 0.64169 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.2010A>C r.(?) p.(Pro670=)


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