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.

3 entries on 1 page. Showing entries 1 - 3.
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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.450-15T>G r.spl? p.? - Parent #2 ACMG VUS g.99006106T>G g.98389643T>G CNGA3 c.450-15T>G - CNGA3_000259 heterozygous PubMed: Solaki 2022 - - Unknown ? - - - - DNA SEQ blood - retinal disease ? PubMed: Solaki 2022 number of independent families: 1 ; number of affected individuals: 1; segregation analysis: both parents: 0, one parent or other relatives: 1; no segregation analysis possible: 0 - - - - - - - - 1 LOVD
+/. 5i c.450-15T>G r.[449_450ins450-14_450-1,449_450ins[450-49_450-16;u;450-14_450-1],450_566del,=] p.[Lys151Cysfs*27,Glu150Aspfs*49,Lys151_Arg189del,=] - Unknown - NA g.99006106T>G g.98389643T>G - - CNGA3_000259 analysis variant in in vitro mini-gene splicing assay PubMed: Reuter 2021 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+?/. 5i c.450-15T>G r.[(449_450ins450-14_450-1,449_450ins[450-49_450-16;u;450-14_450-1],450_566del,=)] p.[(Lys151Cysfs*27,Glu150Aspfs*49,Lys151_Arg189del,=)] - Unknown ACMG likely pathogenic (recessive) g.99006106T>G g.98389643T>G - - CNGA3_000259 effect on RNA predicted from in vitro mini-gene splicing assay; ACMG PM2_Moderate, PP3_supporting, PS3_Strong - VCV001064482 - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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