chr17:48272794:C>T Detail (hg19) (COL1A1)

Information

Genome

Assembly Position
hg19 chr17:48,272,794-48,272,794
hg38 chr17:50,195,433-50,195,433 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000088.3:c.1200+1G>A
Ensemble ENST00000225964.10:c.1200+1G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 120150 OMIM
HGNC 2197 HGNC
Ensembl ENSG00000108821 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2011-08-18 criteria provided, single submitter osteogenesis imperfecta germline Detail
Pathogenic 2023-06-22 criteria provided, single submitter Osteogenesis imperfecta type I germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.316 osteogenesis imperfecta NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000088.4(COL1A1):c.1200+1G>A AND Osteogenesis imperfecta ClinVar Detail
NM_000088.4(COL1A1):c.1200+1G>A AND Osteogenesis imperfecta type I ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs72648320 dbSNP
Genome
hg19
Position
chr17:48,272,794-48,272,794
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser