Full data view for gene LAMB2

Information The variants shown are described using the NM_002292.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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     
+?/. - c.4276dup r.(?) p.(Ala1426Glyfs*6) - Both (homozygous) ACMG likely pathogenic (recessive) g.49160434dup g.49123001dup - - LAMB2_000122 ACMG PVS1,PM2 PubMed: Anazi 2017 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel ID 14DG1320 PubMed: Anazi 2017 simplex case M - - - - - - - 1 Johan den Dunnen
+/. - c.4276dup r.(?) p.(Ala1426Glyfs*6) - Both (homozygous) ACMG pathogenic (recessive) g.49160434dup g.49123001dup - - LAMB2_000122 ACMG PVS1, PM2, PP1 PubMed: Patel 2017 - - Germline - - - - - DNA SEQ-NG - - MCOP F18‐M PubMed: Patel 2017 patient - - Saudi Arabia - - - - - 1 LOVD
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