Full data view for gene FGF20

Information The variants shown are described using the NM_019851.2 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.150C>A r.(?) p.(Gly50=) Unknown - likely benign g.16859392G>T - FGF20(NM_019851.2):c.150C>A (p.G50=) - FGF20_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.181C>A r.(?) p.(His61Asn) Unknown - VUS g.16859361G>T g.17001852G>T FGF20(NM_019851.2):c.181C>A (p.(His61Asn)) - FGF20_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.183C>G r.(?) p.(His61Gln) Unknown - VUS g.16859359G>C g.17001850G>C FGF20(NM_019851.2):c.183C>G (p.(His61Gln)) - FGF20_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.210T>C r.(?) p.(Tyr70=) Unknown - benign g.16859332A>G - FGF20(NM_019851.2):c.210T>C (p.Y70=) - FGF20_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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