Variant #0000570860 (NC_000021.8:g.46875982G>A, NM_030582.3:c.538G>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.46875982G>A
DNA change (hg38) g.45456068G>A
Published as COL18A1(NM_030582.3):c.538G>A (p.(Ala180Thr)), COL18A1(NM_030582.4):c.538G>A (p.A180T)
ISCN -
DB-ID COL18A1_000162 See all 2 reported entries
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) 0.00728 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL18A1 NM_030582.3 -?/. - c.538G>A r.(?) p.(Ala180Thr)


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