"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SARS2"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559226	NM_017827.4(SARS2):c.1541A>T (p.Gln514Leu)	SARS2 (Q514L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 559227	NM_017827.4(SARS2):c.1539C>G (p.Gly513=)	SARS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 215115	NM_017827.4(SARS2):c.1530_1538dup (p.Leu511_Gly513dup)	SARS2	Duplication (inframe_insertion)	not provided	GBenign
Select item 3380616	NM_017827.4(SARS2):c.1414_1415delinsCT (p.Asp472Leu)	SARS2 (D472L +1 more)	Indel (missense variant)	not provided	GUncertain significance
Select item 559229	NM_017827.4(SARS2):c.1347+9C>T	SARS2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 559230	NM_017827.4(SARS2):c.1317C>T (p.Thr439=)	SARS2	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 329212	NM_017827.4(SARS2):c.1160+4T>C	SARS2	Single nucleotide variant (intron variant)	Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome +1 more	GBenign
Select item 1196088	NM_017827.4(SARS2):c.637G>A (p.Asp213Asn)	SARS2 (D213N +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 138958	NM_017827.4(SARS2):c.590-5T>A	SARS2	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 559231	NM_017827.4(SARS2):c.352C>T (p.Arg118Trp)	SARS2 (R118W)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 3380617	NM_017827.4(SARS2):c.337G>A (p.Val113Met)	SARS2 (V113M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 329224	NM_017827.4(SARS2):c.321G>A (p.Glu107=)	SARS2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 138959	NM_017827.4(SARS2):c.273G>A (p.Ser91=)	SARS2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 138961	NM_017827.4(SARS2):c.248C>T (p.Ser83Leu)	LOC130064387, SARS2 (S83L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 138960	NM_017827.4(SARS2):c.103A>G (p.Thr35Ala)	LOC130064387, SARS2 (T35A)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 329226	NM_017827.4(SARS2):c.44G>C (p.Arg15Pro)	LOC130064387, SARS2 (R15P)	Single nucleotide variant (missense variant)	Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome +1 more	GUncertain significance