Variant #0000305048 (NC_000002.11:g.223161799C>T, NM_181457.3:c.219G>A (PAX3))

Chromosome 2
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.223161799C>T
DNA change (hg38) g.222297080C>T
Published as PAX3(NM_181458.3):c.219G>A (p.S73=)
ISCN -
DB-ID PAX3_000133
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-10-28 17:50:42 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC140 NM_153038.1 -?/. - c.-1451C>T r.(?) p.(=)
PAX3 NM_181457.3 -?/. - c.219G>A r.(?) p.(Ser73=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.