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     
+/. 2 c.130_151dup r.(?) p.(Ala51fs*15) - Both (homozygous) - pathogenic g.98994178_98994199del - - - CNGA3_000045 Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. Sharon, submitted - - Germline - - - - - DNA SEQ - - ACHM3 - Sharon, submitted - F yes Israel Arab-Muslim - - - - 2 Dror Sharon
+/. - c.130_151dup r.(?) p.(Ala51Valfs*16) - Unknown ACMG pathogenic g.98994178_98994199dup - c.130_151dup22 - CNGA3_000045 - PubMed: Sharon 2019 - - Germline - 5/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 5 IRD families - - Israel - - - - - 5 Global Variome, with Curator vacancy
+/. 3 c.130_151dup r.130_151dup p.(Ala51Valfs*16) - Both (homozygous) - pathogenic (recessive) g.98994178_98994199dup g.98377715_98377736dup - - CNGA3_000045 - PubMed: Fadaie 2021 - - Unknown yes - - - - DNA SEQ-NG - - retinal disease ? Fadaie 2021, submitted - F - Israel - - - - - 1 Zeinab Fadaie
+?/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Both (homozygous) - likely pathogenic g.98994178_98994199dup g.98377715_98377736dup c.130_151dup22 / c.130 151dup22 - CNGA3_000045 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0177-3 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Both (homozygous) - likely pathogenic g.98994178_98994199dup g.98377715_98377736dup c.130_151dup22 / c.130 151dup22 - CNGA3_000045 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0177-4 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Both (homozygous) - likely pathogenic g.98994178_98994199dup g.98377715_98377736dup c.130_151dup22 I c.130 151dup22 - CNGA3_000045 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0527-1 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Both (homozygous) - likely pathogenic g.98994178_98994199dup g.98377715_98377736dup c.130_151dup22 I c.130 151dup22 - CNGA3_000045 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0527-2 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Both (homozygous) - likely pathogenic g.98994178_98994199dup g.98377715_98377736dup c.130_151dup22 I c.130 151dup22 - CNGA3_000045 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0527-3 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+?/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Both (homozygous) - likely pathogenic g.98994178_98994199dup g.98377715_98377736dup c.130_151dup22 I c.130_151dup22 - CNGA3_000045 homozygous PubMed: Zelinger 2015y - - Germline yes - - - - DNA SEQ blood - retinal disease MOL0586-1 PubMed: Zelinger 2015 - - yes Israel Arab-Muslim - - - - 1 LOVD
+/. - c.130_151dup r.(?) p.(Ala51ValfsTer16) - Parent #2 ACMG pathogenic (recessive) g.98994178_98994199dup g.98377715_98377736dup - - CNGA3_000045 ACMG PVS1, PM2_sup, PS4_sup, PM3_sup PubMed: Andersen 2023 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel ACHM Pat76 PubMed: Andersen 2023 patient - no Denmark - - - - - 1 Susanne Kohl
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