Full data view for gene PRCD

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_001077620.2 transcript reference sequence.

18 entries on 1 page. Showing entries 1 - 18.
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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     
+/. - 
c.64C>T r.(?) p.(Arg22Ter) Parent #2 - pathogenic (recessive) g.74536287C>T g.76540205C>T - - PRCD_000006 - PubMed: Van Huet 2015 - - Germline - - - - - DNA PE, SEQ - APEX retinal disease - PubMed: Van Huet 2015 - - - Netherlands - - - - - 1 LOVD
+/. - c.64C>T r.(?) p.(Arg22Ter) Unknown - pathogenic g.74536287C>T g.76540205C>T - - PRCD_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - pathogenic g.74536287C>T g.76540205C>T - - PRCD_000006 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs387907268 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
+/. - c.64C>T r.(?) p.(Arg22*) Unknown ACMG pathogenic g.74536287C>T - - - PRCD_000006 - PubMed: Sharon 2019 - - Germline - 15/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 15 IRD families - - Israel - - - - - 15 Global Variome, with Curator vacancy
+/. - c.64C>T r.(?) p.(Arg22*) Unknown - pathogenic g.74536287C>T g.76540205C>T - - PRCD_000006 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 164 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+/. 1 c.64C>T r.(?) p.(Arg22Ter) Both (homozygous) - pathogenic (recessive) g.74536287C>T g.76540205C>T - - PRCD_000006 - PubMed: Beheshtian 2015 - - Germline yes - - - - DNA SEQ, SEQ-NG - WES retinal disease 9200034/I-39360 PubMed: Beheshtian 2015 4-generation family, 2 affected (2M), unaffected heterozygous carrier parents/relatives M yes Iran - - - - - 2 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 307 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 308 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 511 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 651 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 616 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 485 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 853 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 572 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 656 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+?/. - c.64C>T r.(?) p.(Arg22*) Both (homozygous) - likely pathogenic g.74536287C>T g.76540205C>T PRCD c.64C>T (p.R22X) - PRCD_000006 homozygous PubMed: Nevet 2010 - - Germline yes - - - - DNA SEQ blood - retinal disease 505 PubMed: Nevet 2010 single village with high carrier frequency; family numbers on pedigrees do not have individual numbers that are in the table ? yes Israel Arab - - - - 1 LOVD
+/. 1 c.64C>T r.(?) p.(Arg22*) Both (homozygous) - pathogenic g.74536287C>T - c.64C>T - PRCD_000006 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. - c.64C>T r.(?) p.(Arg22Ter) Both (homozygous) ACMG pathogenic (recessive) g.74536287C>T g.76540205C>T - - PRCD_000006 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? ARRP-435 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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