Variant #0000707011 (NC_000007.13:g.94034006G>T, NM_000089.3:c.326G>T (COL1A2))

Chromosome 7
Allele Paternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.94034006G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A2_000682
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ken Poole
Database submission license No license selected
Created by Ken Poole
Date created 2019-02-07 13:55:14 +01:00 (CET)
Date last edited 2021-10-11 22:40:40 +02:00 (CEST)
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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 +?/+ 8 c.326G>T r.(?) p.(Gly109Val) missense -



Screenings

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