Variant #0000570212 (NC_000020.10:g.61457552G>T, NC_000020.10(NM_001853.3):c.685-4G>T (COL9A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61457552G>T
DNA change (hg38) g.62826200G>T
Published as COL9A3(NM_001853.3):c.685-4G>T (p.?), COL9A3(NM_001853.4):c.685-4G>T
ISCN -
DB-ID COL9A3_000051 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) 0.00598 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 20:46:36 +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.685-4G>T r.spl? p.?
TCFL5 NM_006602.2 -/. - c.*15775C>A r.(=) p.(=)


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