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.
Legend   How to query  

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     
?/. 3 c.184C>T r.(?) p.(Pro62Ser) Unknown - likely pathogenic g.94577112G>A g.94111556G>A - - ABCA4_000051 - PubMed: Zernant 2014 - - Germline - - - - - DNA SEQ-NG-I - - STGD1 - PubMed: Zernant 2014 - - - United States African American - - - - 1 Jana Zernant
+?/. 3 c.184C>T r.(?) p.(Pro62Ser) Unknown - likely pathogenic g.94577112G>A g.94111556G>A c.184C>T - ABCA4_000051 - PubMed: Zernant 2011 - - Germline ? - - - - DNA PE, SEQ-NG, SEQ - APEX ? - PubMed: Zernant 2011 - ? ? - ? - - - - 1 Stéphanie Cornelis
+/. 3 c.184C>T r.(?) p.(Pro62Ser) Unknown - pathogenic g.94577112G>A g.94111556G>A c.184C>T - ABCA4_000051 - PubMed: Duno 2012 - - Germline ? - - - - DNA MLPA, PE, MCA, PCR, SEQ - APEX ? - PubMed: Duno 2012 - ? ? Denmark Scandinavian - - - - 1 Stéphanie Cornelis
+?/. 3 c.184C>T r.(184c>u) p.(Pro62Ser) Parent #1 ACMG likely pathogenic (recessive) g.94577112G>A g.94111556G>A - - ABCA4_000051 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 - - - - - - - - - - - - - - - - - - - - - - -
?/. 3 c.184C>T r.(?) p.(Pro62Ser) Unknown - VUS g.94577112G>A g.94111556G>A c.184C>T (p.Pro62Ser) - ABCA4_000051 no variant 2nd chromosome; no segregation analysis done PubMed: Zernant 2017 - - Unknown - - - - - DNA SEQ-NG-I - - retinal disease 3103 PubMed: Zernant 2017 - - ? United States - - - - - 1 Stéphanie Cornelis
?/. 3 c.184C>T r.(?) p.(Pro62Ser) Unknown - VUS g.94577112G>A g.94111556G>A c.184C>T, p.Pro62Ser Heterozygous - ABCA4_000051 no variant 2nd chromosome PubMed: Goetz 2020 - - Unknown - - - - - DNA SEQ - - retinal disease 1041-2468 PubMed: Goetz 2020 - - ? - - - - - - 1 Stéphanie Cornelis
+?/. 3 c.184C>T r.(?) p.(Pro62Ser) Parent #1 - likely pathogenic g.94577112G>A - c.184C>T - ABCA4_000051 - PubMed: Maggi_2021 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Maggi_2021 - M - Switzerland - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.