Variant #0000959670 (NC_000007.13:g.94033880C>T, NM_000089.3:c.292C>T (COL1A2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.94033880C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A2_000982
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs765868569
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-01-31 10:34:01 +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     

Predicted     

Legacy protein change     
COL1A2 NM_000089.3 +?/. - c.292C>T r.(?) p.(Pro98Ser) - -


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