Variant #0000836763 (NC_000011.9:g.93913262G>C, NM_015368.3:c.1040G>C (PANX1))

Chromosome 11
Allele Paternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.93913262G>C
DNA change (hg38) g.94180096G>C
Published as -
ISCN -
DB-ID PANX1_000010 See all 2 reported entries
Variant remarks in vitro expression PANX1 showed altered glycosylation (reduced GLY1, absent GLY2)
Reference PubMed: Sang 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-01-31 09:12:52 +01:00 (CET)
Date last edited 2022-01-31 09:18:24 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PANX1 NM_015368.3 +/. - c.1040G>C - p.Cys347Ser


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