Variant #0000254958 (NC_000019.9:g.7600899A>G, NM_006702.4:c.108A>G (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.7600899A>G
DNA change (hg38) g.7536013A>G
Published as PNPLA6(NM_001166111.1):c.252A>G (p.R84=)
ISCN -
DB-ID PNPLA6_000010
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) 0.00016 View details
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 2020-07-15 11:03:00 +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.108A>G r.(?) p.(Arg36=)
MCOLN1 NM_020533.2 -?/. - c.*2218A>G r.(=) p.(=)


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