Variant #0000578417 (NC_000020.10:g.61468571T>C, NM_001853.3:c.1740T>C (COL9A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61468571T>C
DNA change (hg38) g.62837219T>C
Published as -
ISCN -
DB-ID COL9A3_000011 See all 4 reported entries
Variant remarks -
Reference PubMed: Asamura 2005
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency 45/300 controls
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.68093 View details
Owner LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-10-21 16:34:54 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A3 NM_001853.3 -/? 30 c.1740T>C r.(?) p.(=)


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