Variant #0000328601 (NC_000020.10:g.61470065G>A, NM_001853.3:c.1816G>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.61470065G>A
DNA change (hg38) g.62838713G>A
Published as COL9A3(NM_001853.3):c.1816G>A (p.(Ala606Thr)), COL9A3(NM_001853.4):c.1816G>A (p.A606T)
ISCN -
DB-ID COL9A3_000028 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) 0.00879 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +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.1816G>A r.(?) p.(Ala606Thr)
TCFL5 NM_006602.2 -?/. - c.*3262C>T r.(=) p.(=)
DPH3P1 NM_080750.3 -?/. - c.-6951G>A r.(?) p.(=)


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