Variant #0000273908 (NC_000021.8:g.46930005_46930006del, NM_030582.3:c.4054_4055del (COL18A1))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46930005_46930006del
DNA change (hg38) g.45510091_45510092del
Published as COL18A1(NM_001379500.1):c.3523_3524del (p.(Leu1175fs)), COL18A1(NM_001379500.1):c.3523_3524delCT (p.L1175Vfs*72), COL18A1(NM_130445.2):c.3514_3515d...
ISCN -
DB-ID COL18A1_000002 See all 12 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) 0.0003 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC19A1 NM_001205206.1 +/. - c.*4884_*4885del r.(=) p.(=)
COL18A1 NM_030582.3 +/. - c.4054_4055del r.(?) p.(Leu1352ValfsTer72)


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