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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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-/- 14 c.1307G>A r.(?) p.(Ser436Asn) Cadherin 4 (349-460) Maternal (confirmed) - benign g.73406232G>A g.71646475G>A - - CDH23_000234 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033369 Germline - 3/876 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 14 c.1307G>A r.(?) p.(Ser436Asn) Cadherin 4 (349-460) Maternal (confirmed) - benign g.73406232G>A g.71646475G>A - - CDH23_000234 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033369 Germline - 3/876 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/. - c.1307G>A r.(?) p.(Ser436Asn) - Unknown - benign g.73406232G>A g.71646475G>A CDH23(NM_022124.5):c.1307G>A (p.S436N), CDH23(NM_022124.6):c.1307G>A (p.S436N) - CDH23_000234 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1307G>A r.(?) p.(Ser436Asn) - Unknown - likely benign g.73406232G>A g.71646475G>A CDH23(NM_022124.5):c.1307G>A (p.S436N), CDH23(NM_022124.6):c.1307G>A (p.S436N) - CDH23_000234 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1307G>A r.(?) p.(Ser436Asn) - Unknown - likely benign g.73406232G>A g.71646475G>A CDH23(NM_022124.5):c.1307G>A (p.S436N), CDH23(NM_022124.6):c.1307G>A (p.S436N) - CDH23_000234 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1307G>A r.(?) p.(Ser436Asn) - Unknown - VUS g.73406232G>A g.71646475G>A - - CDH23_000234 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case29303 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - 1 LOVD
-/. - c.1307G>A r.(?) p.(Ser436Asn) - Unknown - benign g.73406232G>A - CDH23(NM_022124.5):c.1307G>A (p.S436N), CDH23(NM_022124.6):c.1307G>A (p.S436N) - CDH23_000234 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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