Variant #0000862515 (NC_000011.9:g.31824263G>T, NM_000280.3:c.130C>A (PAX6))

Chromosome 11
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.31824263G>T
DNA change (hg38) -
Published as PAX6(NM_000280.4):c.130C>A (p.(Arg44=)), PAX6(NM_001310158.1):c.130C>A (p.R44=), PAX6(NM_001368910.2):c.373C>A (p.R125=)
ISCN -
DB-ID PAX6_000763 See all 3 reported entries
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) 0.00045 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAX6 NM_000280.3 -?/. - c.130C>A r.(?) p.(=)


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