"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GRIPAP1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2660496	NM_020137.5(GRIPAP1):c.1706G>A (p.Arg569Gln)	GRIPAP1 (R569Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 871499	NM_020137.5(GRIPAP1):c.1544T>C (p.Val515Ala)	GRIPAP1 (V515A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2660497	NM_020137.5(GRIPAP1):c.939A>G (p.Leu313=)	GRIPAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 810592	NM_020137.5(GRIPAP1):c.895C>T (p.Arg299Trp)	GRIPAP1 (R299W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 810593	NM_020137.5(GRIPAP1):c.107T>C (p.Val36Ala)	GRIPAP1 (V36A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	AWAT2, BCLAF3 +568 more	Copy number gain	not provided	GUncertain significance

ClinVar