Variant #0000328587 (NC_000020.10:g.61448942_61448950del, NM_001853.3:c.102_110del (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.61448942_61448950del
DNA change (hg38) g.62817590_62817598del
Published as COL9A3(NM_001853.3):c.90_98del (p.(Gly32_Pro34del))
ISCN -
DB-ID COL9A3_000073
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A3 NM_001853.3 ?/. - c.102_110del r.(?) p.(Pro39_Gly41del)
TCFL5 NM_006602.2 ?/. - c.*24389_*24397del r.(=) p.(=)
OGFR NM_007346.2 ?/. - c.*3941_*3949del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.