Variant #0000328604 (NC_000020.10:g.61477100G>A, NM_001853.3:c.*5016G>A (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.61477100G>A
DNA change (hg38) g.62845748G>A
Published as DPH3P1(NM_080750.4):c.85G>A (p.(Gly29Arg))
ISCN -
DB-ID DPH3P1_000002
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) 2.0E-5 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 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.*5016G>A r.(=) p.(=)
TCFL5 NM_006602.2 ?/. - c.1381-3651C>T r.(=) p.(=)
DPH3P1 NM_080750.3 ?/. - c.85G>A r.(?) p.(Gly29Arg)


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