Variant #0001051099 (NC_000002.11:g.223161694C>T, NC_000002.11(NM_181457.3):c.321+3G>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.223161694C>T
DNA change (hg38) -
Published as PAX3(NM_181458.4):c.321+3G>A
ISCN -
DB-ID CCDC140_000017
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 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC140 NM_153038.1 -?/. - c.-1556C>T r.(?) p.(=)
PAX3 NM_181457.3 -?/. - c.321+3G>A r.spl? p.?


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