Full data view for gene FLNB

Information The variants shown are described using the NM_001457.3 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     
+/? 3 c.572C>T r.(?) p.(Pro191Leu) Actin binding domain Parent #1 - pathogenic g.58064474C>T g.58078747C>T - - FLNB_000064 - - - - De novo - - - - - DNA SEQ - - LRS - - - - - - - - - - - 1 Stephen Robertson
?/. - c.572C>T r.(?) p.(Pro191Leu) - Unknown - VUS g.58064474C>T - FLNB(NM_001164317.1):c.572C>T (p.P191L) - FLNB_000064 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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