Variant #0000895526 (NC_000021.8:g.46930004_46930006del, NM_030582.3:c.4053_4055del (COL18A1))

Chromosome 21
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.46930004_46930006del
DNA change (hg38) -
Published as COL18A1(NM_130444.3):c.4767_4769delCCT (p.G1590del)
ISCN -
DB-ID COL18A1_000325
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 2026-01-20 18:57:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC19A1 NM_001205206.1 ?/. - c.*4884_*4886del r.(=) p.(=)
COL18A1 NM_001379500.1 ?/. - c.3522_3524del r.(?) p.(Leu1175del)
COL18A1 NM_030582.3 ?/. - c.4053_4055del r.(?) p.(Leu1352del)


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