Variant #0000895523 (NC_000021.8:g.46897879G>A, NM_030582.3:c.1761G>A (COL18A1))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46897879G>A
DNA change (hg38) -
Published as COL18A1(NM_001379500.1):c.1221G>A (p.P407=)
ISCN -
DB-ID COL18A1_000323
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) 0.00011 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
COL18A1 NM_001379500.1 -?/. - c.1221G>A r.(?) p.(Pro407=)
COL18A1 NM_030582.3 -?/. - c.1761G>A r.(?) p.(Pro587=)


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