"GeneDx"[submitter] AND "AGT"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 57820	GRCh38/hg38 1q42.13-42.2(chr1:230489657-231243203)x3	AGT, ARV1 +36 more	Copy number gain	See cases	GUncertain significance
Select item 60111	GRCh38/hg38 1q42.2(chr1:230693760-230780212)x1	AGT, CAPN9 +3 more	Copy number loss	See cases	GPathogenic
Select item 1125579	NM_001384479.1(AGT):c.1345C>T (p.Arg449Cys)	AGT (R449C)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2177676	NM_001384479.1(AGT):c.1207C>A (p.Gln403Lys)	AGT (Q403K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 296076	NM_000029.4(AGT):c.1125-13A>G	AGT	Single nucleotide variant	not provided +1 more	GBenign
Select item 1280906	NM_001384479.1(AGT):c.1098-114G>T	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226630	NM_001384479.1(AGT):c.1098-186T>C	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288046	NM_001384479.1(AGT):c.1097+170T>C	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276076	NM_001384479.1(AGT):c.1097+120C>T	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228271	NM_001384479.1(AGT):c.1097+118C>T	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 254725	NC_000001.11:g.230705941T>C	AGT	Single nucleotide variant	not provided +4 more	GBenign/Likely benign
Select item 429714	NM_001384479.1(AGT):c.1060C>T	AGT	Single nucleotide variant	Essential hypertension, genetic +2 more	GPathogenic/Likely pathogenic
Select item 1231565	NM_001384479.1(AGT):c.829+186C>T	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 429788	NM_001384479.1(AGT):c.829+1G>T	AGT	Single nucleotide variant (splice donor variant)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 18068	NC_000001.11:g.230710048A>G	AGT	Single nucleotide variant	not specified +2 more	GBenign
Select item 296083	NM_000029.4(AGT):c.620C>T (p.Thr207Met)	AGT	Single nucleotide variant	not provided +1 more	GBenign
Select item 1306360	NM_001384479.1(AGT):c.380C>T (p.Pro127Leu)	AGT (P127L)	Single nucleotide variant (missense variant)	Essential hypertension, genetic +2 more	GUncertain significance
Select item 876868	NM_000029.4(AGT):c.127C>T (p.Leu43Phe)	AGT	Single nucleotide variant	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1247694	NM_001384479.1(AGT):c.-30-80A>G	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235229	NM_001384479.1(AGT):c.-30-244G>A	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258430	NM_001384479.1(AGT):c.-31+1130G>A	AGT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 296090	NM_001382817.3(AGT):c.-30-3273G>A	AGT	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 296092	NM_001382817.3(AGT):c.-30-3287A>C	AGT	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 296097	NM_001382817.3(AGT):c.-30-3484G>A	AGT	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

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Items: 25