LOVD - Variant listings for COL1A2

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Patient data (#0001273)
Patient ID
Disease OI IV
Reference Pollitt et al., 2006
Template DNA
Technique SEQ
Remarks This patient is described in Parmar et al., 2007.
Ethnic origin -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 16
DNA change c.767G>T   (View in UCSC Genome Browser, Ensembl)
dbSNP dbSNP
Type Substitution
Mutation effect Missense
Protein p.(Gly256Val)
Legacy change Gly166Val
RNA change -
Re-site -
DB-ID COL1A2_00015

1 entry in COL1A2

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
dbSNP Descending
Ascending
Type Descending
Ascending
Mutation effect Descending
Ascending
Protein Descending
Ascending
Legacy change Descending
Ascending
RNA change Descending
Ascending
Re-site Descending
Ascending
DB-ID Descending
Ascending
+/+ Unknown 16 c.767G>T dbSNP Substitution Missense p.(Gly256Val) Gly166Val - - COL1A2_00015