"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DHFR"[gene - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1658200	NM_000791.4(DHFR):c.471T>C (p.Tyr157=)	DHFR	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 757843	NM_000791.4(DHFR):c.-334T>G	DHFR, MSH3	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +3 more	GLikely benign
Select item 710428	NM_000791.4(DHFR):c.-349G>A	DHFR, MSH3	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 1114240	NM_002439.5(MSH3):c.147T>C (p.Pro49=)	DHFR, MSH3	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 710203	NM_000791.4(DHFR):c.-406CGCTGCAGC[1]	DHFR, MSH3	Microsatellite (5 prime UTR variant +2 more)	not specified +3 more	GBenign/Likely benign
Select item 718446	NM_000791.4(DHFR):c.-418GGCCGCTGC[3]	DHFR, MSH3	Microsatellite (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 2655571	NM_002439.5(MSH3):c.178CCCCCAGCG[3] (p.Ala59_Ala60insProProAlaProProAlaProProAla)	DHFR, MSH3	Microsatellite (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 730678	NM_000791.4(DHFR):c.-411G>A	DHFR, MSH3 (A58V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +2 more	GBenign/Likely benign
Select item 725804	NM_000791.4(DHFR):c.-419C>G	DHFR, MSH3 (A61P)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +2 more	GBenign/Likely benign
Select item 1789977	NM_002439.5(MSH3):c.234C>T (p.His78=)	MSH3, DHFR	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign