Variant #0000836766 (NC_000011.9:g.93913036A>G, NM_015368.3:c.814A>G (PANX1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.93913036A>G
DNA change (hg38) g.94179870A>G
Published as I272V
ISCN -
DB-ID PANX1_000012
Variant remarks in vitro expression PANX1 shows normal glycosylation (GLY1/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) 0.1025 View details
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 09:17:13 +01:00 (CET)
Date last edited 2022-01-31 09:20:00 +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.814A>G - p.Ile272Val


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