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.

14 entries on 1 page. Showing entries 1 - 14.
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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     

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Gender     

Consanguinity     

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Age at death     

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Owner     
+/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - pathogenic g.94476417C>T g.94010861C>T E1885K - ABCA4_000416 - PubMed: Rivera 2000 - - Germline yes - - - - DNA DGGE, DHPLC, SSCA, PCR, SEQ - - STGD1 - PubMed: Rivera 2000 - ? ? Germany ? - - - - 1 Stéphanie Cornelis
+?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - likely pathogenic g.94476417C>T g.94010861C>T G1977S - ABCA4_000416 - PubMed: Rivera 2000 - - Germline yes - - - - DNA DGGE, DHPLC, SSCA, PCR, SEQ - - STGD1 - PubMed: Rivera 2000 - ? ? Germany ? - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - VUS g.94476417C>T g.94010861C>T c.5653G>A - ABCA4_000416 - PubMed: Rosenberg 2007 - - Germline - - - - - DNA PCR, SSCA, PE, SEQ - APEX ? - PubMed: Rosenberg 2007 Mutations were described per allele, not per patient. Therefore, it is possible that another mutation was found on the other chromosome. ? no - ? - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - VUS g.94476417C>T g.94010861C>T c.5653G>A - ABCA4_000416 - PubMed: Rosenberg 2007 - - Germline - - - - - DNA PCR, SSCA, PE, SEQ - APEX ? - PubMed: Rosenberg 2007 Mutations were described per allele, not per patient. Therefore, it is possible that another mutation was found on the other chromosome. ? no - ? - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - VUS g.94476417C>T g.94010861C>T c.5653G>A - ABCA4_000416 - PubMed: Rosenberg 2007 - - Germline - - - - - DNA PCR, SSCA, PE, SEQ - APEX ? - PubMed: Rosenberg 2007 Mutations were described per allele, not per patient. Therefore, it is possible that another mutation was found on the other chromosome. ? no - ? - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Parent #1 - VUS g.94476417C>T g.94010861C>T c.5714+5G>A c.5653G>A - ABCA4_000416 - PubMed: Rosenberg 2007 - - Germline - - - - - DNA PCR, SSCA, PE, SEQ - APEX ? - PubMed: Rosenberg 2007 Mutations were described per allele, not per patient. Therefore, it is possible that another mutation was found on the other chromosome. ? no - ? - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Parent #1 - VUS g.94476417C>T g.94010861C>T c.5714+5G>A c.5653G>A - ABCA4_000416 - PubMed: Rosenberg 2007 - - Germline - - - - - DNA PCR, SSCA, PE, SEQ - APEX ? - PubMed: Rosenberg 2007 Mutations were described per allele, not per patient. Therefore, it is possible that another mutation was found on the other chromosome. ? no - ? - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Parent #1 - VUS g.94476417C>T g.94010861C>T c.5714+5G>A c.5653G>A - ABCA4_000416 - PubMed: Rosenberg 2007 - - Germline - - - - - DNA PCR, SSCA, PE, SEQ - APEX ? - PubMed: Rosenberg 2007 Mutations were described per allele, not per patient. Therefore, it is possible that another mutation was found on the other chromosome. ? no - ? - - - - 1 Stéphanie Cornelis
+?/. 40 c.5653G>A r.(5653g>a) p.(Glu1885Lys) Parent #1 ACMG likely pathogenic (recessive) g.94476417C>T g.94010861C>T - - ABCA4_000416 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.5653G>A r.(?) p.(Glu1885Lys) Unknown - pathogenic g.94476417C>T g.94010861C>T - - ABCA4_000416 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs62642563 Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Parent #1 - VUS g.94476417C>T - 5653G>A (E1885 K) - ABCA4_000416 - PubMed: Scholl 2001 - - Germline yes - - - - DNA SSCA, SEQ, DGGE - - retinal disease - PubMed: Scholl 2001 - M - - - - - - - 1 Julia Lopez
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - VUS g.94476417C>T g.94010861C>T p.E1885K - ABCA4_000416 no variant 2nd chromosome; no segregation analysis done PubMed: Jiang 2016 - - Unknown - - - - - DNA PCR, SEQ - - retinal disease 10025 PubMed: Jiang 2016 - - ? China - - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - VUS g.94476417C>T g.94010861C>T c.5653G>A p.(Glu1885Lys) - ABCA4_000416 no variant 2nd chromosome PubMed: Koyanagi 2019 - - Unknown - - - - - DNA SEQ-NG-I - - retinal disease Unknown 1262 PubMed: Koyanagi 2019 mutations were not reported per patient. - ? - Japan - - - - 1 Stéphanie Cornelis
?/. 40 c.5653G>A r.(?) p.(Glu1885Lys) Unknown - VUS g.94476417C>T g.94010861C>T E1885K - ABCA4_000416 - PubMed: Scholl 2001 - - Unknown - - - - - DNA DGGE, DHPLC, SSCA, SEQ - - retinal disease 3 PubMed: Scholl 2001 - M no - - - - - - 1 Stéphanie Cornelis
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