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.

5 entries on 1 page. Showing entries 1 - 5.
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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.458C>T r.(?) p.(Thr153Met) - Paternal (confirmed) ACMG likely benign g.99006129C>T g.98389666C>T CNGA3 c.458C>T, p.(Thr153Met) - CNGA3_000185 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-432 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband M - Spain - - - - - 1 LOVD
-?/. - c.458C>T r.(?) p.(Thr153Met) - Paternal (confirmed) ACMG likely benign g.99006129C>T g.98389666C>T CNGA3 c.458C>T, p.(Thr153Met) - CNGA3_000185 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-433 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband's sister F - Spain - - - - - 1 LOVD
-?/. - c.458C>T r.(?) p.(Thr153Met) - Paternal (confirmed) ACMG likely benign g.99006129C>T g.98389666C>T CNGA3 c.458C>T, p.(Thr153Met) - CNGA3_000185 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-432 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband M - Spain - - - - - 1 LOVD
-?/. - c.458C>T r.(?) p.(Thr153Met) - Paternal (confirmed) ACMG likely benign g.99006129C>T g.98389666C>T CNGA3 c.458C>T, p.(Thr153Met) - CNGA3_000185 - PubMed: Rodriguez Munoz 2021 - - Germline yes - - - - DNA SEQ-NG blood custom panel of 117 IRD-associated genes retinal disease RPN-433 PubMed: Rodriguez Munoz 2021 family ID fRPN-194, proband's sister F - Spain - - - - - 1 LOVD
-/. - c.458C>T r.(?) p.(Thr153Met) - Parent #1 ACMG benign g.99006129C>T g.98389666C>T CNGA3 c.[458C>T;1585G>A] - CNGA3_000185 heterozygous PubMed: Solaki 2022 - - Germline yes - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 2; segregation analysis: both parents: 0, one parent or other relatives: 2; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
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