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     
+?/? 11i c.999+5G>C r.spl? p.(=) Both (homozygous) - likely pathogenic g.35473775C>G g.35505998C>G c.999+5G>C - TULP1_000017 - PubMed: den Hollander 2007 - - Germline - - - - - DNA arraySNP, PCR, SEQ - - LCA15 - PubMed: den Hollander 2007 ? M yes Turkey - - - - - 1 Raheel Qamar
+?/. - c.999+5G>C r.spl p.? Both (homozygous) - benign g.35473775C>G - - - TULP1_000017 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 homozygous patient - - Norway - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.999+5G>C r.(?) p.? Paternal (confirmed) - likely pathogenic (recessive) g.35473775C>G g.35505998C>G - - TULP1_000017 - PubMed: Thompson 2017 - - Germline - - - - - DNA SEQ - - retinal disease Fam2175 PubMed: Thompson 2017 family, 2 affected - - Australia - - - - - 2 LOVD
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