Variant #0000618271 (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) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61468571T>C
DNA change (hg38) g.62837219T>C
Published as COL9A3(NM_001853.4):c.1740T>C (p.P580=)
ISCN -
DB-ID COL9A3_000011 See all 4 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) 0.68093 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.1740T>C r.(?) p.(Pro580=)
TCFL5 NM_006602.2 -/. - c.*4756A>G r.(=) p.(=)
DPH3P1 NM_080750.3 -/. - c.-8445T>C r.(?) p.(=)


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