Full data view for gene POC1B

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_172240.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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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.987C>A r.(?) p.(Tyr329*) Maternal (confirmed) - pathogenic (recessive) g.89860592G>T g.89466815G>T C987A - POC1B_000021 - PubMed: Kominami 2019, PubMed: Kominami 2017, Journal: Kominami 2017 - - Germline - - - 0 - DNA SEQ, SEQ-NG Blood WES COD patient PubMed: Kominami 2019, PubMed: Kominami 2017, Journal: Kominami 2017 2-generation family, 1 affected, unaffected parents M no Japan - >20y 0 - - 1 Najlae Akhiyate
+/. - c.987C>A r.(?) p.(Tyr329*) Maternal (confirmed) - pathogenic (recessive) g.89860592G>T - C987A - POC1B_000021 - PubMed: Kominami 2017, PubMed: Kominami 2017 - - Germline - - - 0 - DNA SEQ Blood - COD patient PubMed: Kominami 2017, PubMed: Kominami 2017 - M no Japan Japan >20y 0 - - 1 Jens Doets
+/. - c.987C>A r.(?) p.(Tyr329*) Maternal (confirmed) - pathogenic (recessive) g.89860592G>T - - - POC1B_000021 - PubMed: Kameya 2019 - - Germline - - - 0 - DNA SEQ - - retinal disease Fam3 PubMed: Kameya 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Japan - - 0 - - 1 LOVD
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