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     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. 26i c.3862+3A>G r.spl? p.(?) Unknown - VUS g.94502293T>C g.94036737T>C - - ABCA4_000588 - PubMed: Alapati 2014 - - Germline - - - - - DNA PE, PCR, SEQ - APEX ? - PubMed: Alapati 2014 - ? ? United States American - - - - 1 Stéphanie Cornelis
?/. 26i c.3862+3A>G r.[=,3814_3862del] p.[=,Ile1272ValfsTer101] Parent #1 ACMG VUS g.94502293T>C g.94036737T>C - - ABCA4_000588 variant significantly enriched in >3000 likely Caucasian STGD1 patients compared to the non-Finnish ExAC population PubMed: Cornelis 2017, Journal: Cornelis 2017, Journal: Cornelis 2023 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3862+3A>G r.spl? p.? Unknown - VUS g.94502293T>C g.94036737T>C - - ABCA4_000588 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 26i c.3862+3A>G r.[=,3814_3862del] p.[(=,Ile1272Valfs∗101)] Unknown - NA g.94502293T>C g.94036737T>C - - ABCA4_000588 expression cloning midigene splicing construct: 0.534 correctly spliced RNA PubMed: Sangermano 2018 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
?/. 26i c.3862+3A>G r.[=,3814_3862del] p.[=,Ile1272Valfs*101] Unknown - VUS g.94502293T>C g.94036737T>C c.IVS26+3A>G=c.3862+3A>G, Heterozygous - ABCA4_000588 no variant 2nd chromosome PubMed: Goetz 2020 - - Unknown - - - - - DNA SEQ - - retinal disease 798-1347 PubMed: Goetz 2020 - - ? - - - - - - 1 Stéphanie Cornelis
?/. 26i c.3862+3A>G r.[=,3814_3862del] p.[=,Ile1272Valfs*101] Unknown - VUS g.94502293T>C g.94036737T>C c.3862+3A>G, Heterozygous - ABCA4_000588 - PubMed: Goetz 2020 - - Unknown - - - - - DNA SEQ - - retinal disease 799-1347 PubMed: Goetz 2020 799 is a family member of 798 - ? - - - - - - 1 Stéphanie Cornelis
?/. 26i c.3862+3A>G r.[=,3814_3862del] p.[=,Ile1272Valfs*101] Unknown - VUS g.94502293T>C g.94036737T>C c.3862+3A>G, Heterozygous - ABCA4_000588 - PubMed: Goetz 2020 - - Unknown - - - - - DNA SEQ - - retinal disease 799-1347 PubMed: Goetz 2020 799 is a family member of 798 - ? - - - - - - 1 Stéphanie Cornelis
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