Variant #0000954006 (NC_000006.11:g.70989351C>A, NC_000006.11(NM_001851.4):c.975+1164G>T (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.70989351C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL9A1_000118
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs993045120
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-12-21 17:11:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A1 NM_001851.4 -?/. - c.975+1164G>T r.(?) p.(?)


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