Variant #0000568839 (NC_000019.9:g.7620614_7620617dup, NM_006702.4:c.2944_2947dup (PNPLA6))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7620614_7620617dup
DNA change (hg38) g.7555728_7555731dup
Published as PNPLA6(NM_001166111.2):c.3088_3091dupAGCC (p.R1031Qfs*38)
ISCN -
DB-ID PNPLA6_000003 See all 4 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNPLA6 NM_006702.4 +?/. - c.2944_2947dup r.(?) p.(Arg983GlnfsTer38)


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