Full data view for gene PCYT1A

Information The variants shown are described using the NM_005017.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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     
+/. 10 c.968dup r.(?) p.(Ser323Argfs*38) Both (homozygous) - pathogenic (recessive) g.195965695dup g.196238824dup - - PCYT1A_000012 - PubMed: Yamamoto 2014, Journal: Yamamoto 2014, OMIM:var0009 - - Germline yes rs587777196 - - - DNA SEQ, SEQ-NG - - SMDCRD - PubMed: Yamamoto 2014, Journal: Yamamoto 2014 5-generation family, 2 affecteds, unaffected carrier parents/relatives, PatV2 F yes Japan - - - - - 2 Johan den Dunnen
+/. 10 c.968dup r.(?) p.(Ser323Argfs*38) Both (homozygous) - pathogenic (recessive) g.195965695dup g.196238824dup - - PCYT1A_000012 - PubMed: Yamamoto 2014, Journal: Yamamoto 2014, OMIM:var0009 - - Germline yes rs587777196 - - - DNA SEQ, SEQ-NG - - SMDCRD - PubMed: Yamamoto 2014, Journal: Yamamoto 2014 PatV5 F yes Japan - - - - - 1 Johan den Dunnen
+?/. - c.968dup r.(?) p.(Ser323Argfs*38) Parent #1 - likely pathogenic g.195965695dup g.196238824dup PCYT1A, variant 1: c.968dup/p.S323Rfs*38, variant 2: c.471C>G/p.F157L - PCYT1A_000012 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 468 PubMed: Weisschuh 2020 Filing key number: 150, Leber congenital amaurosis, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
Legend   How to query  


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