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)     

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     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.67-1G>C r.spl p.? Parent #2 - likely pathogenic g.94578623C>G g.94113067C>G IVS1-1G>C - ABCA4_001481 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 668 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+/. 1i c.67-1G>C r.spl p.? Unknown - pathogenic (recessive) g.94578623C>G g.94113067C>G c.67-1G>C p.(I23Afs*24) - ABCA4_001481 no variant 2nd chromosome PubMed: Schulz 2017 - - Unknown - - - - - DNA arraySEQ, SEQ-NG - RetChip retinal disease Unknown 375 PubMed: Schulz 2017 191 F, 144 M in this study - ? Germany - - - - - 1 Stéphanie Cornelis
+/. 1i c.67-1G>C r.spl p.? Unknown - pathogenic (recessive) g.94578623C>G g.94113067C>G c.67-1G>C, splice sitealteration - ABCA4_001481 no variant 2nd chromosome PubMed: Fujinami 2019 - - Unknown - - - - - DNA SEQ-NG - SEQ-NG (143 cases), APEX (44 cases), SSCP (24 cases), SEQ (134) retinal disease 17034 PubMed: Fujinami 2019 191 F, 154 M in this study - ? United States - - - - - 1 Stéphanie Cornelis
+/. 1i c.67-1G>C r.spl p.? Unknown - pathogenic (recessive) g.94578623C>G g.94113067C>G c.67-1G>C, Heterozygous - ABCA4_001481 no variant 2nd chromosome PubMed: Goetz 2020 - - Unknown - - - - - DNA SEQ-NG-I - solid state SBS retinal disease 2774-4353 PubMed: Goetz 2020 - - ? - - - - - - 1 Stéphanie Cornelis
+/. 1i c.67-1G>C r.spl p.? Parent #2 - pathogenic (recessive) g.94578623C>G g.94113067C>G c.67-1G>C IVS1-1 G>C - ABCA4_001481 - PubMed: Stone 2017 - - Unknown yes - - - - DNA SEQ-NG-I - - retinal disease 668 PubMed: Stone 2017 - M ? - - - - - - 1 Stéphanie Cornelis
+?/. - c.67-1G>C r.spl p.? Unknown - likely pathogenic (recessive) g.94578623C>G g.94113067C>G - - ABCA4_001481 no variant 2nd chromosome PubMed: Cornelis 2024, Journal: Cornelis 2024 - - Unknown - - - - - DNA DHPLC, SEQ - - retinal disease L-0816 PubMed: Cornelis 2024, Journal: Cornelis 2024 - M - France - - - - - 1 Frans Cremers
+?/. 1i c.67-1G>C r.spl p.? Unknown ACMG likely pathogenic g.94578623C>G g.94113067C>G - - ABCA4_001481 ACMG PVS1, PM2_sup; severity category severe Journal: Cornelis 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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