Variant #0000983698 (NC_000019.9:g.7600768G>A, NC_000019.9(NM_006702.4):c.28-51G>A (PNPLA6))

Chromosome 19
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.7600768G>A
DNA change (hg38) -
Published as PNPLA6(NM_001166111.1):c.121G>A (p.G41S), PNPLA6(NM_001166114.2):c.94G>A (p.(Gly32Ser))
ISCN -
DB-ID PNPLA6_000009 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) 0.00037 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNPLA6 NM_006702.4 -?/. - c.28-51G>A r.(=) p.(=)
MCOLN1 NM_020533.2 -?/. - c.*2087G>A r.(=) p.(=)


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