Full data view for gene MATN3

Information The variants shown are described using the NM_002381.4 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
-/. 2 c.526G>T r.(?) p.(Val176Leu) - Paternal (confirmed) - benign g.20205769C>A g.20006008C>A g.11687G>T - MATN3_000031 - - - rs200762092 Germline yes - - - - DNA SEQ-NG-I blood - CM1 @VED - - F no Italy White - - - Surgery of cranial posterior fossa 3 Patrizia De Marco
?/. - c.526G>T r.(?) p.(Val176Leu) - Unknown - VUS g.20205769C>A g.20006008C>A MATN3(NM_002381.4):c.526G>T (p.V176L, p.(Val176Leu)) - MATN3_000031 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.526G>T r.(?) p.(Val176Leu) - Unknown - likely benign g.20205769C>A - MATN3(NM_002381.4):c.526G>T (p.V176L, p.(Val176Leu)) - MATN3_000031 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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