Full data view for gene ARHGAP4

Information The variants shown are described using the NM_001666.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.941C>G r.(?) p.(Pro314Arg) Unknown - VUS g.153184377G>C g.153918923G>C ARHGAP4(NM_001164741.1):c.1061C>G (p.P354R, p.(Pro354Arg)) - ARHGAP4_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.941C>G r.(?) p.(Pro314Arg) Unknown - likely benign g.153184377G>C g.153918923G>C ARHGAP4(NM_001164741.1):c.1061C>G (p.P354R, p.(Pro354Arg)) - ARHGAP4_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
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