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.

7 entries on 1 page. Showing entries 1 - 7.
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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.872C>G r.(?) p.(Thr291Arg) - Parent #1 - likely pathogenic g.99012505C>G g.98396042C>G CNGA3, variant 1: c.872C>G/p.T291R, variant 2: c.1641C>A/p.F547L - CNGA3_000177 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 19 PubMed: Weisschuh 2020 Filing key number: 11, achromatopsia, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.872C>G r.(?) p.(Thr291Arg) - Parent #1 - likely pathogenic g.99012505C>G g.98396042C>G CNGA3, variant 1: c.872C>G/p.T291R, variant 2: c.1641C>A/p.F547L - CNGA3_000177 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 20 PubMed: Weisschuh 2020 Filing key number: 11, achromatopsia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. 7 c.872C>G r.(?) p.(Thr291Arg) - Parent #1 - likely pathogenic g.99012505C>G g.98396042C>G allele 1/2: T291R/F547L - CNGA3_000177 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO11/L PubMed: Wissinger 2001 - F - Germany - - - - - 1 LOVD
+?/. 7 c.872C>G r.(?) p.(Thr291Arg) - Parent #1 - likely pathogenic g.99012505C>G g.98396042C>G allele 1/2: T291R/F547L - CNGA3_000177 heterozygous PubMed: Wissinger 2001 - - Germline yes - - - - DNA SEQ, SSCA blood direct DNA sequencing or SSCP retinal disease CHRO11/W PubMed: Wissinger 2001 - M - Germany - - - - - 1 LOVD
+?/. - c.872C>G r.(?) p.(Thr291Arg) - Parent #1 - likely pathogenic g.99012505C>G g.98396042C>G CNGA3 nt912 C>G (exon 7), Thr291Arg - CNGA3_000177 old nucleotide numbering system, c. annotations extrapolated from literature and databases PubMed: Kohl 1998 - - Germline yes - - - - DNA SEQ - - retinal disease ACHR11_1 PubMed: Kohl 1998 sibling of ACHR11_2 - - Germany - - - - - 1 LOVD
+?/. - c.872C>G r.(?) p.(Thr291Arg) - Parent #1 - likely pathogenic g.99012505C>G g.98396042C>G CNGA3 nt912 C>G (exon 7), Thr291Arg - CNGA3_000177 old nucleotide numbering system, c. annotations extrapolated from literature and databases PubMed: Kohl 1998 - - Germline yes - - - - DNA SEQ - - retinal disease ACHR11_2 PubMed: Kohl 1998 sibling of ACHR11_1 - - Germany - - - - - 1 LOVD
+/. - c.872C>G r.(?) p.(Thr291Arg) - Parent #2 ACMG pathogenic g.99012505C>G g.98396042C>G CNGA3 c.872C>G - CNGA3_000177 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: 2, one parent or other relatives: 0; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
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