Related gene-specific medical variations for Gene (Select 641518) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3118306	NM_016269.5(LEF1):c.91G>C (p.Asp31His)	LEF1, LEF1-AS1 (D31H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623984	NM_016269.5(LEF1):c.73C>T (p.Pro25Ser)	LEF1, LEF1-AS1 (P25S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279310	NM_016269.5(LEF1):c.38G>A (p.Gly13Glu)	LEF1, LEF1-AS1 (G13E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1319981	NM_016269.5(LEF1):c.66GAT[3] (p.Met23dup)	LEF1, LEF1-AS1	Microsatellite (inframe_insertion +1 more)	Ectrodactyly and ectodermal dysplasia without cleft lip/palate	GPathogenic
Select item 242785	NM_016269.5(LEF1):c.133G>A (p.Glu45Lys)	LEF1, LEF1-AS1 (E45K)	Single nucleotide variant (missense variant +1 more)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 242717	NM_016269.5(LEF1):c.181T>C (p.Ser61Pro)	LEF1, LEF1-AS1 (S61P)	Single nucleotide variant (missense variant +1 more)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 14382	NM_016269.4(LEF1):c.[133G>A;181T>C]	LEF1, LEF1-AS1 (S61P +1 more)	Single nucleotide variant (missense variant +1 more)	Sebaceous tumors, somatic	GPathogenic

ClinVar