"Ambry Genetics"[submitter] AND "AGTR2"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 11716	NM_000686.5(AGTR2):c.62G>T (p.Gly21Val)	AGTR2 (G21V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2309091	NM_000686.5(AGTR2):c.76T>C (p.Ser26Pro)	AGTR2 (S26P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1764352	NM_000686.5(AGTR2):c.86A>G (p.Asn29Ser)	AGTR2 (N29S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097433	NM_000686.5(AGTR2):c.90G>C (p.Glu30Asp)	AGTR2 (E30D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356532	NM_000686.5(AGTR2):c.109C>G (p.Gln37Glu)	AGTR2 (Q37E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557360	NM_000686.5(AGTR2):c.145A>G (p.Ile49Val)	AGTR2 (I49V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3276709	NM_000686.5(AGTR2):c.154T>G (p.Tyr52Asp)	AGTR2 (Y52D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097387	NM_000686.5(AGTR2):c.170T>C (p.Ile57Thr)	AGTR2 (I57T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381705	NM_000686.5(AGTR2):c.211T>A (p.Cys71Ser)	AGTR2 (C71S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2243695	NM_000686.5(AGTR2):c.314C>G (p.Ser105Cys)	AGTR2 (S105C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1740391	NM_000686.5(AGTR2):c.440T>A (p.Ile147Asn)	AGTR2 (I147N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 590238	NM_000686.5(AGTR2):c.498T>C (p.Leu166=)	AGTR2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 3097397	NM_000686.5(AGTR2):c.532A>G (p.Thr178Ala)	AGTR2 (T178A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392175	NM_000686.5(AGTR2):c.550G>A (p.Val184Ile)	AGTR2 (V184I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261652	NM_000686.5(AGTR2):c.601C>T (p.Pro201Ser)	AGTR2 (P201S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230452	NM_000686.5(AGTR2):c.665T>C (p.Ile222Thr)	AGTR2 (I222T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550470	NM_000686.5(AGTR2):c.711C>G (p.His237Gln)	AGTR2 (H237Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 93332	NM_000686.5(AGTR2):c.743G>A (p.Arg248Lys)	AGTR2 (R248K)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1762116	NM_000686.5(AGTR2):c.812C>T (p.Pro271Leu)	AGTR2 (P271L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097424	NM_000686.5(AGTR2):c.878T>C (p.Ile293Thr)	AGTR2 (I293T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315084	NM_000686.5(AGTR2):c.902C>T (p.Pro301Leu)	AGTR2 (P301L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543460	NM_000686.5(AGTR2):c.926C>A (p.Thr309Asn)	AGTR2 (T309N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 590237	NM_000686.5(AGTR2):c.1011T>A (p.Ile337=)	AGTR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 23