Variant #0000000369 (NC_000007.13:g.127253856C>T, NM_006193.2:c.492G>A (PAX4))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.127253856C>T
Reference -
DB-ID PAX4_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00014 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-07-18 08:48:53 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAX4 NM_006193.2 +/+ 4 c.492G>A r.(=) p.(=)