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     

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Age at death     

VIP     

Data_av     

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Panel size     

Owner     
?/. - c.2470A>C r.(?) p.(Ser824Arg) Parent #1 - VUS g.153174934T>G g.153909480T>G - - ARHGAP4_000043 recurrent, found 2 times PubMed: Tarpey 2009 - - Germline - 2/208 cases - 0 - DNA SEQ - - MRX;IDX 19377476-Pat? PubMed: Tarpey 2009 - M - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - 2 Lucy Raymond
-?/. - c.2470A>C r.(?) p.(Ser824Arg) Unknown - likely benign g.153174934T>G g.153909480T>G ARHGAP4(NM_001164741.1):c.2590A>C (p.(Ser864Arg)) - ARHGAP4_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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