Variant #0000895416 (NC_000020.10:g.61468587A>C, NM_001853.3:c.1756A>C (COL9A3))

Chromosome 20
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.61468587A>C
DNA change (hg38) -
Published as COL9A3(NM_001853.3):c.1756A>C (p.(Thr586Pro))
ISCN -
DB-ID COL9A3_000119
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) 0.00031 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A3 NM_001853.3 ?/. - c.1756A>C r.(?) p.(Thr586Pro)
TCFL5 NM_006602.2 ?/. - c.*4740T>G r.(=) p.(=)
DPH3P1 NM_080750.3 ?/. - c.-8429A>C r.(?) p.(=)


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