"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MSR1"[g - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 712059	NM_138715.3(MSR1):c.1194C>T (p.Ala398=)	MSR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 782031	NM_138715.3(MSR1):c.1128C>T (p.Asp376=)	MSR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 778941	NM_138715.3(MSR1):c.1038A>G (p.Pro346=)	MSR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 746739	NM_138715.3(MSR1):c.1034-8C>A	MSR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2075747	NM_138715.3(MSR1):c.1034-19_1034-10del	MSR1	Deletion (intron variant)	not provided	GLikely benign
Select item 782854	NM_138715.3(MSR1):c.1034-15_1034-10del	MSR1	Deletion (intron variant)	not provided	GLikely benign
Select item 2776135	NM_138715.3(MSR1):c.1034-11del	MSR1	Deletion (intron variant)	not provided	GBenign
Select item 714374	NM_138715.3(MSR1):c.1033+10T>C	MSR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 714511	NM_138715.3(MSR1):c.1014G>A (p.Lys338=)	MSR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 14357	NM_138715.3(MSR1):c.877C>T (p.Arg293Ter)	MSR1 (R293* +1 more)	Single nucleotide variant (nonsense)	Malignant tumor of prostate +3 more	GConflicting classifications of pathogenicity
Select item 773758	NM_138715.3(MSR1):c.630+3A>G	MSR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 729324	NM_138715.3(MSR1):c.542T>A (p.Ile181Lys)	MSR1 (I199K +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 747968	NM_138715.3(MSR1):c.103+1G>T	MSR1	Single nucleotide variant (splice donor variant)	not provided	GLikely benign