Variant #0000997736 (NC_000009.11:g.140446853G>A, NM_001098537.1:c.-2204C>T (PNPLA7))

Chromosome 9
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.140446853G>A
DNA change (hg38) -
Published as MRPL41(NM_032477.2):c.320G>A (p.(Gly107Asp))
ISCN -
DB-ID MRPL41_000005
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) 1.0E-5 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 2024-08-28 13:16:32 +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     
PNPLA7 NM_001098537.1 ?/. - c.-2204C>T r.(?) p.(=)
MRPL41 NM_032477.2 ?/. - c.320G>A r.(?) p.(Gly107Asp)
WDR85 NM_138778.2 ?/. - c.*2838C>T r.(=) p.(=)


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