Full data view for gene ATF6

Information The variants shown are described using the NM_007348.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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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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Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.1110dup r.(?) p.(Val371SerfsTer3) Parent #2 - likely pathogenic (recessive) g.161790874dup g.161821084dup - - ATF6_000024 - PubMed: Weisschuh 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease CHRO436 PubMed: Weisschuh 2016 family - - Germany - - - - - 1 LOVD
+?/. - c.1110dup r.(?) p.(Val371Serfs*3) Parent #1 - likely pathogenic g.161790874dup g.161821084dup ATF6, variant 1: c.797dup/p.N267*, variant 2: c.1110dup/p.V371Sfs*3 - ATF6_000024 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 968 PubMed: Weisschuh 2020 Filing key number: 436, achromatopsia, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.1110dup r.(?) p.(Val371Serfs*3) Parent #1 - likely pathogenic g.161790874dup g.161821084dup ATF6, variant 1: c.797dup/p.N267*, variant 2: c.1110dup/p.V371Sfs*3 - ATF6_000024 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 969 PubMed: Weisschuh 2020 Filing key number: 436, achromatopsia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.1110dupA r.(?) p.(Val371Serfs*3) Paternal (confirmed) - likely pathogenic g.161790874dup g.161821084dup ATF6 c.1110dupA, p.(Val371Serfs*3) - ATF6_000024 compound heterozygous PubMed: Kohl 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO436-II:1 PubMed: Kohl 2015 Family CHRO436, patient II:1 M - - German - - - - 1 LOVD
+?/. - c.1110dupA r.(?) p.(Val371Serfs*3) Paternal (confirmed) - likely pathogenic g.161790874dup g.161821084dup ATF6 c.1110dupA, p.(Val371Serfs*3) - ATF6_000024 compound heterozygous PubMed: Kohl 2015 - - Germline yes - - - - DNA SEQ blood - retinal disease CHRO436-II:2 PubMed: Kohl 2015 Family CHRO436, patient II:2 F - - German - - - - 1 LOVD
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