Full data view for gene MVK

In collaboration with the Infevers autoinflammatory disorders (AID) databases.
Information The variants shown are described using the NM_000431.2 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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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.803T>C r.(?) p.(Ile268Thr) Unknown - pathogenic g.110029080T>C g.109591275T>C MVK(NM_000431.2):c.803T>C (p.I268T), MVK(NM_000431.4):c.803T>C (p.I268T) - MVK_000115 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.803T>C r.(?) p.(Ile268Thr) Unknown - pathogenic g.110029080T>C g.109591275T>C MVK(NM_000431.2):c.803T>C (p.I268T), MVK(NM_000431.4):c.803T>C (p.I268T) - MVK_000115 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.803T>C r.(?) p.(Ile268Thr) Unknown - pathogenic g.110029080T>C g.109591275T>C MVK(NM_000431.2):c.803T>C (p.I268T), MVK(NM_000431.4):c.803T>C (p.I268T) - MVK_000115 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.803T>C r.(?) p.(Ile268Thr) Unknown - pathogenic g.110029080T>C - MVK(NM_000431.2):c.803T>C (p.I268T), MVK(NM_000431.4):c.803T>C (p.I268T) - MVK_000115 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.803T>C r.(?) p.(Ile268Thr) Unknown ACMG likely pathogenic g.110029080T>C g.109591275T>C MVK:NM_000431 c.T803C, p.I268T - MVK_000115 heterozygous, individual solved, variant non-causal PubMed: Rodriguez-Munoz 2020 - - Germline ? - - - - DNA SEQ-NG-I blood - retinal disease RPN-402 PubMed: Rodriguez-Munoz 2020 family fRPN-183, proband F - Spain - - - - - 1 LOVD
+/. - c.803T>C r.(?) p.(Ile268Thr) Maternal (confirmed) - pathogenic g.110029080T>C g.109591275T>C MVK c.803T>C (p.I268T) - MVK_000115 heterozygous PubMed: Siemiatkowska 2013 - - Germline yes - - - - DNA SEQ-NG, SEQ blood exome sequencing retinal disease A-II:1 PubMed: Siemiatkowska 2013 family A, proband's older brother M - Netherlands white - - - - 1 LOVD
+/. - c.803T>C r.(?) p.(Ile268Thr) Maternal (confirmed) - pathogenic g.110029080T>C g.109591275T>C MVK c.803T>C (p.I268T) - MVK_000115 heterozygous PubMed: Siemiatkowska 2013 - - Germline yes - - - - DNA SEQ-NG, SEQ blood exome sequencing retinal disease A-II:2 PubMed: Siemiatkowska 2013 family A, proband F - Netherlands white - - - - 1 LOVD
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