Variant #0001043641 (NC_000021.8:g.46917558G>C, NM_030582.3:c.3206G>C (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.46917558G>C
DNA change (hg38) -
Published as COL18A1(NM_001379500.1):c.2666G>C (p.(Gly889Ala))
ISCN -
DB-ID COL18A1_000362
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 2025-05-05 21:14:00 +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.2666G>C r.(?) p.(Gly889Ala)
COL18A1 NM_030582.3 ?/. - c.3206G>C r.(?) p.(Gly1069Ala)


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