"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 36576	NM_000251.3(MSH2):c.339G>A (p.Lys113=)	MSH2	Single nucleotide variant (synonymous variant)	Lynch syndrome	GBenign
Select item 439908	NM_000251.3(MSH2):c.942+27_942+29del	MSH2	Deletion (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 374958	NM_000251.3(MSH2):c.942+29del	MSH2	Deletion (intron variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 336428	NM_000251.3(MSH2):c.942+26_942+29del	MSH2	Deletion (intron variant)	Hereditary nonpolyposis colorectal neoplasms +5 more	GConflicting classifications of pathogenicity
Select item 336427	NM_000251.3(MSH2):c.942+28_942+29del	MSH2	Deletion (intron variant)	Lynch syndrome 1 +6 more	GConflicting classifications of pathogenicity
Select item 36580	NM_000251.3(MSH2):c.942+3A>T	MSH2	Single nucleotide variant (intron variant)	Lynch syndrome	GPathogenic
Select item 1762	NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	MSH2 (G322D +1 more)	Single nucleotide variant (missense variant)	Lynch syndrome	GBenign
Select item 91269	NM_000251.3(MSH2):c.984C>T (p.Ala328=)	MSH2	Single nucleotide variant (synonymous variant)	Lynch syndrome	GLikely benign
Select item 36565	NM_000251.3(MSH2):c.1387-8G>T	MSH2	Single nucleotide variant (intron variant)	Lynch syndrome 1	GBenign
Select item 36570	NM_000251.3(MSH2):c.1737A>G (p.Lys579=)	MSH2	Single nucleotide variant (synonymous variant)	Lynch syndrome	GLikely benign
Select item 90910	NM_000251.3(MSH2):c.2154A>G (p.Gln718=)	MSH2	Single nucleotide variant (synonymous variant)	Lynch syndrome	GLikely benign