Full data view for gene GIPC3

Information The variants shown are described using the NM_133261.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

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     
+/+ 2 c.241C>T r.(?) p.(Leu81Phe) Parent #1 - pathogenic g.3586508C>T g.3586510C>T - - GIPC3_000017 - MORL Deafness Variation Database - - SUMMARY record - - - - - DNA ? - - HL - - - - - - - - - - - 1 Global Variome, with Curator vacancy
+/. - c.241C>T r.(?) p.(Leu81Phe) Both (homozygous) ACMG pathogenic (recessive) g.3586508C>T g.3586510C>T - - GIPC3_000017 - PubMed: Wonkam 2022 - rs1487341857 Germline yes - - - - DNA SEQ, SEQ-NG-I Blood WES DFNB15 Fam10 PubMed: Wonkam 2022 3 generation family, 2 affected sisters F no Ghana Africa - - - - 2 Yacouba Dia
+/. - c.241C>T r.(?) p.(Leu81Phe) Both (homozygous) ACMG pathogenic (recessive) g.3586508C>T g.3586510C>T - - GIPC3_000017 unaffected heterozygous mother, one unaffected sister is homozygous for the pathogenic variant, father was no screened. PubMed: Wonkam 2022 - rs1487341857 Germline - - - - - DNA SEQ, SEQ-NG-I Blood WES DFNB15 Fam31 PubMed: Wonkam 2022 3-generation family, 2 affected (1M, 1F), unaffected carrier mother, unaffected homozygous sister M no Ghana Africa - - - - 2 Yacouba Dia
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.