Full data view for gene CDH23


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_022124.5 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
-?/? 35 c.4216A>G r.(?) p.(Ile1406Val) Cadherin 13 (1314-1418) Unknown ACMG likely benign g.73498261A>G g.71738504A>G - - CDH23_000414 heterozygous; uncertain PubMed: Mizutari 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs192459984 Germline - 1/189 controls hmutai - - DNA SEQ - - DFN - PubMed: Mizutari 2015 Proband F - Japan Asian-Japanese - - - - 1 Hideki Mutai
-?/. - c.4216A>G r.(?) p.(Ile1406Val) - Unknown - likely benign g.73498261A>G g.71738504A>G CDH23(NM_022124.5):c.4216A>G (p.I1406V) - CDH23_000414 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. 33 c.4216A>G r.(?) p.(Ile1406Val) - Unknown - VUS g.73498261A>G g.71738504A>G A4216G - CDH23_000414 - PubMed: Katagiri 2014 - rs192459984 Germline - - - - - DNA SEQ-NG - WES retinal disease RP#003 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
?/. 33 c.4216A>G r.(?) p.(Ile1406Val) - Unknown - VUS g.73498261A>G g.71738504A>G A4216G - CDH23_000414 - PubMed: Katagiri 2014 - rs192459984 Germline - - - - - DNA SEQ-NG - WES retinal disease RP#011 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
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