Variant #0000618264 (NC_000020.10:g.61448435T>A, NM_001853.3:c.19T>A (COL9A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61448435T>A
DNA change (hg38) g.62817083T>A
Published as COL9A3(NM_001853.3):c.19T>A (p.(Cys7Ser))
ISCN -
DB-ID COL9A3_000081
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) 0.00012 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A3 NM_001853.3 -?/. - c.19T>A r.(?) p.(Cys7Ser)
TCFL5 NM_006602.2 -?/. - c.*24892A>T r.(=) p.(=)
OGFR NM_007346.2 -?/. - c.*3434T>A r.(=) p.(=)


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