All variants in the RAC1 gene

Information The variants shown are described using the NM_018890.3 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
+?/. - c.116A>G r.(?) p.(Asn39Ser) - likely pathogenic g.6431563A>G g.6391932A>G - - RAC1_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
-/. - c.225+18C>T r.(=) p.(=) - benign g.6431690C>T g.6392059C>T RAC1(NM_018890.3):c.225+18C>T - RAC1_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_AMC
-?/. - c.240_241insT r.(?) p.(Gly81TrpfsTer2) - likely benign g.6438307_6438308insT g.6398676_6398677insT - - RAC1_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
?/. - c.401C>A r.(?) p.(Thr134Asn) - VUS g.6441554C>A - RAC1(NM_018890.3):c.401C>A (p.T134N) - RAC1_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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