Variant #0000689783 (NC_000006.11:g.70976444A>G, NM_001851.4:c.1317T>C (COL9A1))

Chromosome 6
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.70976444A>G
DNA change (hg38) -
Published as COL9A1(NM_001851.4):c.1317T>C (p.G439=), COL9A1(NM_001851.6):c.1317T>C (p.G439=), COL9A1(NM_078485.4):c.588T>C (p.G196=)
ISCN -
DB-ID COL9A1_000090 See all 3 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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A1 NM_001851.4 -?/. - c.1317T>C r.(?) p.(Gly439=)


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