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.

12 entries on 1 page. Showing entries 1 - 12.
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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     
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease IV:3 PubMed: Saqib 2011 family 50 M yes - - - - - - 1 LOVD
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease V:2 PubMed: Saqib 2011 family 50 F yes - - - - - - 1 LOVD
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease V:3 PubMed: Saqib 2011 family 50 F yes - - - - - - 1 LOVD
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease V:4 PubMed: Saqib 2011 family 50 F yes - - - - - - 1 LOVD
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease VI:1 PubMed: Saqib 2011 family 50 M yes - - - - - - 1 LOVD
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease VI:2 PubMed: Saqib 2011 family 50 F yes - - - - - - 1 LOVD
+?/. 7 c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G c.827A>G, p.N276S - CNGA3_000213 homozygous PubMed: Saqib 2011 - - Germline yes - - - - DNA SEQ blood Exome sequencing retinal disease VI:3 PubMed: Saqib 2011 family 50 F yes - - - - - - 1 LOVD
+?/. - c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G CNGA3 c.827A>G, p.(Asn276Ser) - CNGA3_000213 homozygous PubMed: Yousaf 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease PKAB149_III:2 PubMed: Yousaf 2022 family PKAB149, individual III:2 M yes Pakistan Pakistani - - - - 1 LOVD
+?/. - c.827A>G r.(?) p.(Asn276Ser) - Both (homozygous) - likely pathogenic g.99012460A>G g.98395997A>G CNGA3 c.827A>G, p.(Asn276Ser) - CNGA3_000213 homozygous PubMed: Yousaf 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease PKAB149_III:3 PubMed: Yousaf 2022 family PKAB149, individual III:3 M yes Pakistan Pakistani - - - - 1 LOVD
+/. - c.827A>G r.(?) p.(Asn276Ser) - Unknown ACMG pathogenic (recessive) g.99012460A>G g.98395997A>G - - CNGA3_000213 ACMG PP3, PM2, PM1, PP2, PP5_STRONG PubMed: Weisschuh 2024 156335 - Germline - - - - - DNA SEQ-NG - WGS ? ACHM-1291 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
+/. - c.827A>G r.(?) p.(Asn276Ser) TM4 Unknown - pathogenic (recessive) g.99012460A>G g.98395997A>G - - CNGA3_000213 ACMG PM1_mod, PP1_sup, PP2_sup, PM2_mod, PP3_sup, PS3_strong PubMed: Solaki 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.827A>G - p.Asn276Ser TM4 Unknown - NA g.99012460A>G g.98395997A>G - - CNGA3_000213 in vitro functional analysis normalized overall luminescence signal (AUC) 0.03±0.01 PubMed: Solaki 2023 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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