Variant #0000892158 (NC_000015.9:g.55759250dup, NM_130810.3:c.523dup (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.55759250dup
DNA change (hg38) -
Published as DNAAF4(NM_130810.4):c.523dupA (p.I175Nfs*15)
ISCN -
DB-ID CCPG1_000018
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C15orf65 NM_001198784.1 +/. - c.*48482dup r.(?) p.(=)
CCPG1 NM_004748.4 +/. - c.-59207dup r.(?) p.(=)
PIGB NM_004855.4 +/. - c.*111620dup r.(?) p.(=)
DYX1C1 NM_130810.3 +/. - c.523dup r.(?) p.(Ile175Asnfs*15)
DYX1C1-CCPG1 NR_037923.1 +/. - n.778dup r.(?) -


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