Variant #0000809112 (NC_000019.9:g.7601138T>C, NM_006702.4:c.177T>C (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.7601138T>C
DNA change (hg38) -
Published as PNPLA6(NM_001166111.2):c.321T>C (p.Y107=)
ISCN -
DB-ID MCOLN1_000038
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +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.177T>C r.(?) p.(Tyr59=)
MCOLN1 NM_020533.2 -?/. - c.*2457T>C r.(=) p.(=)


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