Full data view for gene CNGA3

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_001298.2 transcript reference sequence.

13 entries on 1 page. Showing entries 1 - 13.
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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     
+?/. - c.488C>T r.(?) p.(Pro163Leu) - Unknown - likely pathogenic g.99006159C>T g.98389696C>T - - CNGA3_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.488C>T r.(?) p.(Pro163Leu) - Parent #1 - pathogenic g.99006159C>T g.98389696C>T - - CNGA3_000030 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs104893612 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
?/. 6 c.488C>T r.(?) p.(Pro163Leu) - Both (homozygous) - VUS g.99006159C>T - c.488C>T - CNGA3_000030 - PubMed: Abu-Safieh-2013 - - Germline - - - - - DNA SEQ-NG blood autozygome-guided sequencing retinal disease - PubMed: Abu-Safieh-2013 - - - Saudi Arabia - - - - - 1 LOVD
+/. - c.488C>T r.(?) p.(Pro163Leu) - Paternal (confirmed) - pathogenic (recessive) g.99006159C>T g.98389696C>T - - CNGA3_000030 - PubMed: Varsanyi 2005 - - Germline - - - - - DNA SEQ - - retinal disease FamEPatIII1 PubMed: Varsanyi 2005 3-generation family, 3 affected (2F, M), unaffected heterozygous carrier relatives F - Hungary - - - - - 3 Johan den Dunnen
+/. - c.488C>T r.(?) p.(Pro163Leu) - Paternal (confirmed) - pathogenic (recessive) g.99006159C>T g.98389696C>T - - CNGA3_000030 - PubMed: Varsanyi 2005 - - Germline - - - - - DNA SEQ - - retinal disease FamEPatIII2 PubMed: Varsanyi 2005 - M - Hungary - - - - - 1 Johan den Dunnen
+?/. 5 c.488C>T r.(?) p.(Pro163Leu) - Both (homozygous) - likely pathogenic g.99006159C>T g.98389696C>T allele 1/2: P163L/P163L - CNGA3_000030 homozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO14/B PubMed: Wissinger 2001 - F - Germany - - - - - 1 LOVD
+?/. 5 c.488C>T r.(?) p.(Pro163Leu) - Parent #1 - likely pathogenic g.99006159C>T g.98389696C>T allele 1/2: P163L/R436W - CNGA3_000030 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO61/198 PubMed: Wissinger 2001 - M - Germany - - - - - 1 LOVD
+?/. - c.488C>T r.(?) p.(Pro163Leu) - Both (homozygous) - likely pathogenic g.99006159C>T g.98389696C>T CNGA3 nt528 C>T (exon 5), Pro163Leu - CNGA3_000030 old nucleotide numbering system, c. annotations extrapolated from literature and databases PubMed: Kohl 1998 - - Germline yes - - - - DNA SEQ - - retinal disease ACHR14_III:3 PubMed: Kohl 1998 - F - Germany - - - - - 1 LOVD
+?/. - c.488C>T r.(?) p.(Pro163Leu) - Both (homozygous) - likely pathogenic g.99006159C>T g.98389696C>T CNGA3 nt528 C>T (exon 5), Pro163Leu - CNGA3_000030 old nucleotide numbering system, c. annotations extrapolated from literature and databases PubMed: Kohl 1998 - - Germline yes - - - - DNA SEQ - - retinal disease ACHR14_III:4 PubMed: Kohl 1998 - M - Germany - - - - - 1 LOVD
+?/. - c.488C>T r.(?) p.(Pro163Leu) - Both (homozygous) - likely pathogenic g.99006159C>T g.98389696C>T CNGA3 nt528 C>T (exon 5), Pro163Leu - CNGA3_000030 old nucleotide numbering system, c. annotations extrapolated from literature and databases PubMed: Kohl 1998 - - Germline yes - - - - DNA SEQ - - retinal disease ACHR14_IV:1 PubMed: Kohl 1998 - M - Germany - - - - - 1 LOVD
+/. - c.488C>T r.(?) p.(Pro163Leu) - Parent #2 ACMG pathogenic g.99006159C>T g.98389696C>T CNGA3 c.488C>T - CNGA3_000030 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 1; segregation analysis: both parents: 1, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.488C>T r.(?) p.(Pro163Leu) - Both (homozygous) ACMG pathogenic g.99006159C>T g.98389696C>T CNGA3 c.488C>T - CNGA3_000030 homozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 2 ; number of affected individuals: 5; segregation analysis: both parents: 3, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. - c.488C>T r.(?) p.(Pro163Leu) - Parent #2 ACMG pathogenic g.99006159C>T g.98389696C>T CNGA3 c.488C>T - CNGA3_000030 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 2 ; number of affected individuals: 3; segregation analysis: both parents: 3, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
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