"Baylor Genetics"[submitter] AND "MLH3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 997548	NM_001040108.2(MLH3):c.3475G>C (p.Asp1159His)	MLH3 (D1159H)	Single nucleotide variant (missense variant)	Colorectal cancer, hereditary nonpolyposis, type 7 +1 more	GUncertain significance
Select item 410889	NM_001040108.2(MLH3):c.2021dup (p.Asn674fs)	MLH3 (N674fs)	Duplication (frameshift variant)	Endometrial carcinoma +2 more	GUncertain significance
Select item 625564	GRCh37/hg19 14q24.3(chr14:74040231-76368547)	ABCD4, ACOT2 +38 more	Copy number loss	not provided	GLikely pathogenic

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