"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SARS2"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559230	NM_017827.4(SARS2):c.1317C>T (p.Thr439=)	SARS2	Single nucleotide variant (synonymous variant)	Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome +1 more	GConflicting classifications of pathogenicity
Select item 808578	NM_017827.4(SARS2):c.1147G>A (p.Gly383Ser)	SARS2 (G383S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2649826	NM_017827.4(SARS2):c.858C>T (p.Ile286=)	SARS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 546839	NM_017827.4(SARS2):c.796G>C (p.Gly266Arg)	SARS2 (G268R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 380990	NM_017827.4(SARS2):c.696C>T (p.Arg232=)	SARS2	Single nucleotide variant (synonymous variant)	Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome +1 more	GBenign/Likely benign
Select item 138958	NM_017827.4(SARS2):c.590-5T>A	SARS2	Single nucleotide variant (intron variant)	SARS2-related condition +3 more	GConflicting classifications of pathogenicity
Select item 138961	NM_017827.4(SARS2):c.248C>T (p.Ser83Leu)	LOC130064387, SARS2 (S83L)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 2649827	NM_017827.4(SARS2):c.142G>A (p.Ala48Thr)	LOC130064387, SARS2 (A48T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1420911	NM_017827.4(SARS2):c.17C>T (p.Ala6Val)	LOC130064387, SARS2 (A6V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity