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.

4 entries on 1 page. Showing entries 1 - 4.
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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.380C>T r.(?) p.(Pro127Leu) Unknown - VUS g.110019208C>T g.109581403C>T MVK(NM_000431.2):c.380C>T (p.P127L) - MVK_000046 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.380C>T r.(?) p.(Pro127Leu) Unknown - pathogenic g.110019208C>T g.109581403C>T - - MVK_000046 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs775474803 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.380C>T r.(?) p.(Pro127Leu) Both (homozygous) - likely pathogenic (recessive) g.110019208C>T g.109581403C>T - - MVK_000046 - PubMed: Taylor 2017 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease 14008687 PubMed: Taylor 2017 no family history retinal disease M - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.380C>T r.(?) p.(Pro127Leu) Both (homozygous) - likely pathogenic g.110019208C>T g.109581403C>T MVK;NM_000431.2;c.[380C>T];[380C>T];p.[(Pro127Leu)];[(Pro127Leu)] - MVK_000046 homozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 56 PubMed: Jiman 2020 - M - (United Kingdom (Great Britain)) - - - - - 1 LOVD
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