Variant #0001005812 (NC_000021.8:g.46925320dup, NM_030582.3:c.3602dup (COL18A1))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46925320dup
DNA change (hg38) -
Published as COL18A1(NM_130445.2):c.3053dupC (p.(Gly1019fs))
ISCN -
DB-ID COL18A1_000353
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL18A1 NM_001379500.1 +?/. - c.3062dup r.(?) p.(Gly1022Trpfs*65)
COL18A1 NM_030582.3 +?/. - c.3602dup r.(?) p.(Gly1202Trpfs*65)


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