Full data view for gene TMEM38B


Osteogenesis Imperfecta Variant Database
Information The variants shown are described using the NM_018112.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 3i c.455-7T>G r.spl p.? Parent #1 - pathogenic (dominant) g.108484808T>G g.105722527T>G - - TMEM38B_000007 - PubMed: Liu 2017 - - Germline - 1/101 cases OI - - - DNA SEQ-NG - targeted 14-gene panel OI OI Fam28 PubMed: Liu 2017 analysis 101 unrelated OI families - - China - - - - - 1 Johan den Dunnen
+/+ 3i c.455-7T>G r.spl p.Arg151_Gly152insValLeu Both (homozygous) - pathogenic g.108484808T>G - - - TMEM38B_000007 shifts the 3ยด splice site by six bases and results in a two-amino-acid insertion PubMed: Lv 2016 - - Germline - - - - - DNA, RNA PCR, RT-PCR, SEQ - - OI Family 1 PubMed: Lv 2016 - - - China Han - - - - 1 Raymond Dalgleish
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