Variant #0000507432 (NC_000001.10:g.40773175G>C, NC_000001.10(NM_001852.3):c.955-4C>G (COL9A2))

Chromosome 1
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.40773175G>C
DNA change (hg38) g.40307503G>C
Published as COL9A2(NM_001852.3):c.955-4C>G (p.?), COL9A2(NM_001852.4):c.955-4C>G
ISCN -
DB-ID COL9A2_000019 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) 0.0272 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-04 12:45:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A2 NM_001852.3 -?/. - c.955-4C>G r.spl? p.?


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