Variant #0000328580 (NC_000020.10:g.61444641_61444699del, NM_001853.3:c.-3776_-3718del (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.61444641_61444699del
DNA change (hg38) g.62813289_62813347del
Published as OGFR(NM_007346.2):c.1672_1730del (p.(Ser559IlefsTer15))
ISCN -
DB-ID OGFR_000012
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) Retrieve
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 2020-07-16 20:41:08 +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.-3776_-3718del r.(?) p.(=)
TCFL5 NM_006602.2 ?/. - c.*28630_*28688del r.(=) p.(=)
OGFR NM_007346.2 ?/. - c.1674_1732del r.(?) p.(Ser559IlefsTer15)


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