Variant #0000570199 (NC_000020.10:g.61449868del, NC_000020.10(NM_001853.3):c.148-2del (COL9A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.61449868del
DNA change (hg38) g.62818516del
Published as -
ISCN -
DB-ID COL9A3_000043
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 20:44:57 +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.148-2del r.spl? p.?
TCFL5 NM_006602.2 +?/. - c.*23459del r.(?) p.(=)
OGFR NM_007346.2 +?/. - c.*4867del r.(?) p.(=)


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