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.

10 entries on 1 page. Showing entries 1 - 10.
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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.62C>G r.(?) p.(Ser21Ter) - Unknown - pathogenic g.98986500C>G g.98370037C>G CNGA3(NM_001298.2):c.62C>G (p.S21*) - CNGA3_000058 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.62C>G r.(?) p.(Ser21Ter) - Parent #1 - likely pathogenic (recessive) g.98986500C>G g.98370037C>G - - CNGA3_000058 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT7 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.62C>G r.(?) p.(Ser21Ter) - Parent #1 - likely pathogenic (recessive) g.98986500C>G g.98370037C>G - - CNGA3_000058 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES retinal disease QT353 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.62C>G r.(?) p.(Ser21Ter) - Both (homozygous) - likely pathogenic (recessive) g.98986500C>G g.98370037C>G - - CNGA3_000058 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT570 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.62C>G r.(?) p.(Ser21Ter) - Parent #1 - likely pathogenic (recessive) g.98986500C>G g.98370037C>G - - CNGA3_000058 - PubMed: Li 2014, PubMed: Huang 2016 - - Germline - - - - - DNA SEQ - - retinal disease QT942 PubMed: Li 2014, PubMed: Huang 2016 see paper ... - - China - - - - - 1 Johan den Dunnen
+?/. - c.62C>G r.(?) p.(Ser21Ter) - Parent #1 - likely pathogenic (recessive) g.98986500C>G g.98370037C>G - - CNGA3_000058 - PubMed: Huang 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease QT1305 PubMed: Huang 2016 - - - China - - - - - 1 Johan den Dunnen
+?/. - c.62C>G r.(?) p.(Ser21*) - Unknown - likely pathogenic g.98986500C>G g.98370037C>G c.62C>G, p.(Ser21*) - CNGA3_000058 compound heterozygous PubMed: Wang 2019 - - Germline yes - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 14415 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.62C>G r.(?) p.(Ser21*) - Unknown - likely pathogenic g.98986500C>G g.98370037C>G CNGA3 c.62C>G(;)128C>A - CNGA3_000058 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 10668 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. - c.62C>G r.(?) p.(Ser21*) - Parent #1 - likely pathogenic g.98986500C>G g.98370037C>G CNGA3 c.[62C>G];[1585G>A] - CNGA3_000058 heterozygous; protein change not reported PubMed: Sun 2020 - - Unknown yes - - - - DNA SEQ-NG blood Whole-exome or targeted sequencing retinal disease 15732 PubMed: Sun 2020 - F - China - - - - - 1 LOVD
+?/. - c.62C>G r.(?) p.(Ser21*) - Parent #1 - likely pathogenic g.98986500C>G g.98370037C>G CNGA3 c.62C>G, p.S31X - CNGA3_000058 error in annotation: should be S21X and not S31X; heterozygous PubMed: Liang 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease F7-II1 PubMed: Liang 2015 - M - China - - - - - 1 LOVD
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