Variant #0000855993 (NC_000021.8:g.46924426_46924427del, NM_030582.3:c.3363_3364insCCCCCCA (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.46924426_46924427del
DNA change (hg38) -
Published as COL18A1(NM_130444.3):c.4069_4077delGGCCCCCCAinsCCCCCCA (p.G1357Pfs*141)
ISCN -
DB-ID COL18A1_000319
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL18A1 NM_001379500.1 +?/. - c.2824_2825del r.(?) p.(Gly942Profs*144)
COL18A1 NM_030582.3 +?/. - c.3363_3364insCCCCCCA r.(?) p.(Gly1122Profs*144)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.