Variant #0001066222 (NC_000015.9:g.55652089C>G, NM_130810.3:c.*70779G>C (DYX1C1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.55652089C>G
DNA change (hg38) -
Published as CCPG1(NM_001204450.2):c.1882G>C (p.(Ala628Pro))
ISCN -
DB-ID CCPG1_000030
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) 0.00107 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 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.-48878C>G r.(?) p.(=)
CCPG1 NM_004748.4 ?/. - c.1882G>C r.(?) p.(Ala628Pro)
PIGB NM_004855.4 ?/. - c.*4459C>G r.(=) p.(=)
DYX1C1 NM_130810.3 ?/. - c.*70779G>C r.(=) p.(=)
DYX1C1-CCPG1 NR_037923.1 ?/. - n.3299G>C r.(?) -


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