Full data view for gene TULP1

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_003322.3 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     
+?/? 14 c.1376T>A r.(?) p.(Ile459Lys) Paternal (confirmed) - likely pathogenic g.35467877A>T g.35500100A>T T->A - TULP1_000002 - PubMed: Hagstrom 1998 - - Germline - - - - - DNA SSCA, PCRdig, SEQ, PAGE - - RPar - PubMed: Hagstrom 1998 2 generation family 1 affected, 5 carrier F no United States - - - - - 1 Raheel Qamar
+/? 14 c.1376T>A r.(?) p.(Ile459Lys) Maternal (confirmed) - pathogenic g.35467877A>T g.35500100A>T c.1376T>A - TULP1_000002 - PubMed: Banerjee 1998 - - Germline - - - - - DNA PCR, SEQ, SSCA, PAGE - - RPar - PubMed: Banerjee 1998 - M no United States - - - - - 1 Raheel Qamar
+?/. - c.1376T>A r.(?) p.(Ile459Lys) Parent #1 - likely pathogenic g.35467877A>T - - - TULP1_000002 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - 1 Global Variome, with Curator vacancy
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