Full data view for gene MATN3

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

7 entries on 1 page. Showing entries 1 - 7.
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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     
+/? 3 c.908C>T r.(?) p.(Thr303Met) - Parent #1 - pathogenic g.20202930G>A g.20003169G>A - - MATN3_000001 - PubMed: Stefansson 2003, OMIM:var0003 - - Unknown - 2/2162 cases - - - DNA SEQ - - OS2 - - - - - - - - - - - 2 LOVD
+/? 3 c.908C>T r.(?) p.(Thr303Met) - Parent #2 - pathogenic g.20202930G>A g.20003169G>A - - MATN3_000001 - PubMed: Stefansson 2003, OMIM:var0003 - - Unknown - 2/2162 cases - - - DNA SEQ - - OS2 - - - - - - - - - - - 2 LOVD
+/? 3 c.908C>T r.(?) p.(Thr303Met) - Parent #1 - pathogenic g.20202930G>A g.20003169G>A - - MATN3_000001 - PubMed: Stefansson 2003, OMIM:var0003 - - Unknown - 43/2162 cases - - - DNA SEQ - - OS2 - - - - - - - - - - - 43 LOVD
?/? 3 c.908C>T r.(?) p.(Thr303Met) - Unknown - VUS g.20202930G>A g.20003169G>A - - MATN3_000001 - - - rs28939676 Unknown - - - - - DNA SEQ - - Healthy/Control - - - - - - - - - - - 1 LOVD
-?/. - c.908C>T r.(?) p.(Thr303Met) - Unknown - likely benign g.20202930G>A g.20003169G>A MATN3(NM_002381.4):c.908C>T (p.(Thr303Met)), MATN3(NM_002381.5):c.908C>T (p.T303M) - MATN3_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.908C>T r.(?) p.(Thr303Met) - Parent #1 - likely benign g.20202930G>A g.20003169G>A - - MATN3_000001 211 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs77245812 Germline - 211/2793 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 211 Mohammed Faruq
-?/. - c.908C>T r.(?) p.(Thr303Met) - Unknown - likely benign g.20202930G>A - MATN3(NM_002381.4):c.908C>T (p.(Thr303Met)), MATN3(NM_002381.5):c.908C>T (p.T303M) - MATN3_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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