Full data view for gene ABCA4


The expert classification of the variants can be found here.

To other Inherited Retinal Disease gene variant database:
Information The variants shown are described using the NM_000350.2 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

Gender     

Consanguinity     

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Age at death     

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Owner     
+?/. 38 c.5338C>G r.(?) p.(Pro1780Ala) Unknown - likely pathogenic g.94480221G>C g.94014665G>C 5338C>G - ABCA4_000176 On its own not significantely found more often in published STGD compared to ExAC (p-value 0.96). However, together with other non-significant variants published related to STGD, they are significantly more often in STGD patients (p-value <0.01). PubMed: Shroyer 2000 - - Germline yes ExAC 14, 121410, 0, 0.0001153 - - - DNA SSCA, HD, SEQ - - STGD1 - PubMed: Lewis 1999 2-generation family, 4 affected F ? United States white - - - - 1 Stéphanie Cornelis
?/. 38 c.5338C>G r.(5338c>g) p.(Pro1780Ala) Parent #1 ACMG VUS g.94480221G>C g.94014665G>C - - ABCA4_000176 variant frequency lower in a group of >3000 likely Caucasian STGD1 patients than in the ExAC non-Finnish population PubMed: Cornelis 2017, Journal: Cornelis 2017, Journal: Cornelis 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.5338C>G r.(?) p.(Pro1780Ala) Unknown - VUS g.94480221G>C g.94014665G>C ABCA4(NM_000350.3):c.5338C>G (p.P1780A) - ABCA4_000176 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.5338C>G r.(?) p.(Pro1780Ala) Parent #2 - likely pathogenic g.94480221G>C g.94014665G>C - - ABCA4_000176 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 790 PubMed: Stone 2017 family, 4 affected F - (United States) - - - - - 4 LOVD
?/. 38 c.5338C>G r.(?) p.(Pro1780Ala) Parent #2 - VUS g.94480221G>C g.94014665G>C c.5338C>G Pro1780Ala CCA>CGA - ABCA4_000176 - PubMed: Stone 2017 - - Unknown yes - - - - DNA SEQ-NG-I - - retinal disease 790 PubMed: Stone 2017 - F ? - - - - - - 1 Stéphanie Cornelis
?/. 38 c.5338C>G r.(?) p.(Pro1780Ala) Unknown - VUS g.94480221G>C g.94014665G>C c.5338C>G/p.P1780A - ABCA4_000176 no segregation analysis done PubMed: Weisschuh 2020 - - Unknown - - - - - DNA SEQ-NG-I - - retinal disease 338 PubMed: Weisschuh 2020 - F ? Germany - - - - - 1 Stéphanie Cornelis
?/. 38 c.5338C>G r.(?) p.(Pro1780Ala) Unknown - VUS g.94480221G>C - c.1099+3A>C &c.5338C>G (unknown configuration) - ABCA4_000176 - PubMed: Fritsche 2012 - - Unknown ? - - - - DNA SEQ - - retinal disease G03-2346 PubMed: Fritsche 2012 The genotypes for the CFH rs1061170, ARMS2 rs10490924 and C3 rs2230199 locations were T/T, T/T, C/C respectively. F ? Germany - - - - - 1 LOVD
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