"Clinical Genetics, Academic Medical Center"[submitter] AND "MLH3"[gen - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 257253	NM_001040108.2(MLH3):c.4335A>G (p.Gln1445=)	MLH3	Single nucleotide variant (synonymous variant)	Colorectal cancer, hereditary nonpolyposis, type 7 +2 more	GBenign
Select item 314371	NM_001040108.2(MLH3):c.3987+15C>T	MLH3	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 416452	NM_001040108.2(MLH3):c.3315C>A (p.Asp1105Glu)	MLH3 (D1105E)	Single nucleotide variant (missense variant)	Colorectal cancer, hereditary nonpolyposis, type 7 +2 more	GBenign/Likely benign
Select item 220963	NM_001040108.2(MLH3):c.2896T>C (p.Ser966Pro)	MLH3 (S966P)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 220674	NM_001040108.2(MLH3):c.2533A>G (p.Ser845Gly)	MLH3 (S845G)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 257252	NM_001040108.2(MLH3):c.2531C>T (p.Pro844Leu)	MLH3 (P844L)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 257251	NM_001040108.2(MLH3):c.2476A>G (p.Asn826Asp)	MLH3 (N826D)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 5561	NM_001040108.2(MLH3):c.2221G>T (p.Val741Phe)	AREL1, MLH3 (V741F)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 314386	NM_001040108.2(MLH3):c.2159A>G (p.Tyr720Cys)	MLH3 (Y720C)	Single nucleotide variant (missense variant)	MLH3-related condition +3 more	GBenign/Likely benign
Select item 5560	NM_001040108.2(MLH3):c.1870G>C (p.Glu624Gln)	MLH3 (E624Q)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 238243	NM_001040108.2(MLH3):c.1258G>A (p.Val420Ile)	MLH3 (V420I)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 220781	NM_001040108.2(MLH3):c.691A>C (p.Lys231Gln)	MLH3 (K231Q)	Single nucleotide variant (missense variant)	Colorectal cancer, hereditary nonpolyposis, type 7 +2 more	GBenign/Likely benign
Select item 238254	NM_001040108.2(MLH3):c.8A>G (p.Lys3Arg)	MLH3 (K3R)	Single nucleotide variant (missense variant)	Colorectal cancer, hereditary nonpolyposis, type 7 +1 more	GBenign/Likely benign