All variants in the ARMCX4 gene

Information The variants shown are described using the NM_001256155.1 transcript reference sequence.

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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.5440_5441insAGGCTC r.(?) p.(Gly1814delinsGluAlaArg) - likely benign g.100749016_100749017insAGGCTC g.101494029_101494030insAGGCTC ARMCX4(NM_001256155.1):c.5440_5441insAGGCTC (p.(Gly1814delinsGluAlaArg)) - ARMCX4_000014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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