"PreventionGenetics, part of Exact Sciences"[submitter] AND "PIWIL1"[g - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049632	NM_004764.5(PIWIL1):c.18A>G (p.Arg6=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GBenign
Select item 3050449	NM_004764.5(PIWIL1):c.78+8C>T	PIWIL1	Single nucleotide variant (intron variant)	PIWIL1-related disorder	GLikely benign
Select item 3056689	NM_004764.5(PIWIL1):c.94T>G (p.Tyr32Asp)	PIWIL1 (Y32D)	Single nucleotide variant (missense variant)	PIWIL1-related disorder	GLikely benign
Select item 3029045	NM_004764.5(PIWIL1):c.132G>T (p.Gly44=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign
Select item 3056802	NM_004764.5(PIWIL1):c.191-4dup	PIWIL1	Duplication (intron variant)	PIWIL1-related disorder	GLikely benign
Select item 3057484	NM_004764.5(PIWIL1):c.279A>G (p.Thr93=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign
Select item 3039186	NM_004764.5(PIWIL1):c.294C>T (p.Asp98=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign
Select item 3060310	NM_004764.5(PIWIL1):c.317-9C>T	PIWIL1	Single nucleotide variant (intron variant)	PIWIL1-related disorder	GBenign
Select item 3040379	NM_004764.5(PIWIL1):c.345C>T (p.Ser115=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign
Select item 3056328	NM_004764.5(PIWIL1):c.735-7C>T	PIWIL1	Single nucleotide variant (intron variant)	PIWIL1-related disorder	GBenign
Select item 3060640	NM_004764.5(PIWIL1):c.1128G>A (p.Leu376=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GBenign
Select item 3039067	NM_004764.5(PIWIL1):c.1255C>T (p.Arg419Cys)	PIWIL1 (R419C)	Single nucleotide variant (missense variant)	PIWIL1-related disorder	GLikely benign
Select item 3041646	NM_004764.5(PIWIL1):c.1503G>A (p.Thr501=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GBenign
Select item 3055830	NM_004764.5(PIWIL1):c.1580G>A (p.Arg527Lys)	PIWIL1 (R527K)	Single nucleotide variant (missense variant)	PIWIL1-related disorder	GBenign
Select item 3056217	NM_004764.5(PIWIL1):c.1779A>G (p.Lys593=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GBenign
Select item 3043022	NM_004764.5(PIWIL1):c.1867-7A>G	PIWIL1	Single nucleotide variant (intron variant)	PIWIL1-related disorder	GLikely benign
Select item 3045433	NM_004764.5(PIWIL1):c.1893C>T (p.Ile631=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign
Select item 3060964	NM_004764.5(PIWIL1):c.2041+8A>G	PIWIL1	Single nucleotide variant (intron variant)	PIWIL1-related disorder	GBenign
Select item 3033233	NM_004764.5(PIWIL1):c.2094C>T (p.Ile698=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign
Select item 3056973	NM_004764.5(PIWIL1):c.2103C>T (p.Arg701=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GBenign
Select item 3052765	NM_004764.5(PIWIL1):c.2403C>T (p.Ser801=)	PIWIL1	Single nucleotide variant (synonymous variant)	PIWIL1-related disorder	GLikely benign

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Items: 21