"University of Washington Department of Laboratory Medicine, Universit - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 223935	NM_003620.4(PPM1D):c.472+77G>A	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223927	NM_003620.4(PPM1D):c.472+314G>A	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223936	NM_003620.4(PPM1D):c.472+1152A>G	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223939	NM_003620.4(PPM1D):c.472+4585C>T	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223937	NM_003620.4(PPM1D):c.473-1294T>C	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223928	NM_003620.4(PPM1D):c.701+366C>T	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223934	NM_003620.4(PPM1D):c.701+3346A>G	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223938	NM_003620.4(PPM1D):c.702-3299C>T	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223929	NM_003620.4(PPM1D):c.702-2064T>C	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223926	NM_003620.4(PPM1D):c.702-21A>G	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223932	NM_003620.4(PPM1D):c.1017+51A>G	PPM1D	Single nucleotide variant (intron variant)	Familial cancer of breast	GLikely benign
Select item 223933	NM_003620.4(PPM1D):c.1017+3929A>C	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223930	NM_003620.4(PPM1D):c.1260+2807G>A	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 223931	NM_003620.4(PPM1D):c.1261-1386A>G	PPM1D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign