"PreventionGenetics, part of Exact Sciences"[submitter] AND "IMPG1"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058808	NM_001563.4(IMPG1):c.2169C>T (p.Asp723=)	IMPG1	Single nucleotide variant (synonymous variant)	IMPG1-related disorder +1 more	GLikely benign
Select item 1115486	NM_001563.4(IMPG1):c.2126A>G (p.Glu709Gly)	IMPG1 (E631G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 961171	NM_001563.4(IMPG1):c.2045-10T>A	IMPG1	Single nucleotide variant (intron variant)	IMPG1-related disorder +1 more	GLikely benign
Select item 3043233	NM_001563.4(IMPG1):c.1962C>T (p.His654=)	IMPG1	Single nucleotide variant (synonymous variant)	IMPG1-related disorder	GLikely benign
Select item 3031111	NM_001563.4(IMPG1):c.1572G>A (p.Leu524=)	IMPG1	Single nucleotide variant (synonymous variant)	IMPG1-related disorder	GLikely benign
Select item 1932916	NM_001563.4(IMPG1):c.1537G>A (p.Glu513Lys)	IMPG1 (E513K +1 more)	Single nucleotide variant (missense variant)	IMPG1-related disorder +1 more	GUncertain significance
Select item 1081847	NM_001563.4(IMPG1):c.1169A>G (p.Asp390Gly)	IMPG1 (D312G +1 more)	Single nucleotide variant (missense variant)	IMPG1-related disorder +1 more	GLikely benign
Select item 1107117	NM_001563.4(IMPG1):c.915G>A (p.Thr305=)	IMPG1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1136784	NM_001563.4(IMPG1):c.777C>T (p.Tyr259=)	IMPG1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1640239	NM_001563.4(IMPG1):c.666+10T>A	IMPG1	Single nucleotide variant (intron variant)	IMPG1-related disorder +1 more	GLikely benign
Select item 1167072	NM_001563.4(IMPG1):c.650C>T (p.Thr217Ile)	IMPG1 (T139I +1 more)	Single nucleotide variant (missense variant)	IMPG1-related disorder +2 more	GBenign
Select item 1122133	NM_001563.4(IMPG1):c.213C>T (p.Ser71=)	IMPG1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign