Variant #0000951380 (NC_000019.9:g.7600726del, NC_000019.9(NM_006702.4):c.28-93del (PNPLA6))

Chromosome 19
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.7600726del
DNA change (hg38) -
Published as PNPLA6(NM_001166111.1):c.79del (p.(Ala27ArgfsTer35))
ISCN -
DB-ID MCOLN1_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNPLA6 NM_006702.4 ?/. - c.28-93del r.(=) p.(=)
MCOLN1 NM_020533.2 ?/. - c.*2045del r.(?) p.(=)


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