"PreventionGenetics, part of Exact Sciences"[submitter] AND "LRRIQ3"[g - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050772	NM_001105659.2(LRRIQ3):c.1573C>T (p.Arg525Cys)	LRRIQ3 (R525C)	Single nucleotide variant (missense variant +1 more)	LRRIQ3-related disorder	GBenign
Select item 775562	NM_001105659.2(LRRIQ3):c.1192A>G (p.Ile398Val)	LRRIQ3 (I398V)	Single nucleotide variant (missense variant)	LRRIQ3-related disorder +1 more	GBenign
Select item 3048136	NM_001105659.2(LRRIQ3):c.1164T>G (p.Thr388=)	LRRIQ3	Single nucleotide variant (synonymous variant)	LRRIQ3-related disorder	GLikely benign
Select item 3059800	NM_001105659.2(LRRIQ3):c.763G>A (p.Ala255Thr)	LRRIQ3 (A255T)	Single nucleotide variant (missense variant)	LRRIQ3-related disorder	GBenign
Select item 3043290	NM_001105659.2(LRRIQ3):c.696A>G (p.Arg232=)	LRRIQ3	Single nucleotide variant (synonymous variant)	LRRIQ3-related disorder	GLikely benign
Select item 2635230	NM_001105659.2(LRRIQ3):c.573+1G>A	LRRIQ3	Single nucleotide variant (splice donor variant)	LRRIQ3-related disorder	GUncertain significance
Select item 3037245	NM_001105659.2(LRRIQ3):c.466C>T (p.His156Tyr)	LRRIQ3 (H156Y)	Single nucleotide variant (missense variant)	LRRIQ3-related disorder	GBenign
Select item 3034775	NM_001105659.2(LRRIQ3):c.160G>A (p.Val54Ile)	LRRIQ3 (V54I)	Single nucleotide variant (missense variant)	LRRIQ3-related disorder	GLikely benign
Select item 3052134	NM_001105659.2(LRRIQ3):c.69A>C (p.Ile23=)	LRRIQ3	Single nucleotide variant (synonymous variant)	LRRIQ3-related disorder	GLikely benign