Variant #0000306039 (NC_000009.11:g.140441821G>A, NM_001098537.1:c.133C>T (PNPLA7))

Chromosome 9
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.140441821G>A
DNA change (hg38) g.137547369G>A
Published as PNPLA7(NM_001098537.3):c.133C>T (p.L45=)
ISCN -
DB-ID PNPLA7_000002
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) 0.00065 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 2020-06-26 13:17:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNPLA7 NM_001098537.1 -?/. - c.133C>T r.(?) p.(Leu45=)
MRPL41 NM_032477.2 -?/. - c.-4618G>A r.(?) p.(=)


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