Variant #0001066224 (NC_000015.9:g.55759341del, NM_130810.3:c.430del (DYX1C1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55759341del
DNA change (hg38) -
Published as -
ISCN -
DB-ID CCPG1_000032
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +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     
C15orf65 NM_001198784.1 +/. - c.*48573del r.(?) p.(=)
CCPG1 NM_004748.4 +/. - c.-59300del r.(?) p.(=)
PIGB NM_004855.4 +/. - c.*111711del r.(?) p.(=)
DYX1C1 NM_130810.3 +/. - c.430del r.(?) p.(Ile144*)
DYX1C1-CCPG1 NR_037923.1 +/. - n.685del r.(?) -


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