Variant #0001015902 (NC_000021.8:g.46914484dup, NM_030582.3:c.2918dup (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.46914484dup
DNA change (hg38) -
Published as COL18A1(NM_001379500.1):c.2378dupC (p.P795Sfs*69)
ISCN -
DB-ID COL18A1_000356
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 2024-10-29 21:08:56 +01:00 (CET)
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.2378dup r.(?) p.(Pro795Serfs*69)
COL18A1 NM_030582.3 +?/. - c.2918dup r.(?) p.(Pro975Serfs*69)


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