"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "FOXI3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1167409	NM_001135649.3(FOXI3):c.889_891dup (p.Thr297dup)	FOXI3	Duplication (inframe_insertion)	not provided	GBenign
Select item 2082977	NM_001135649.3(FOXI3):c.872C>T (p.Pro291Leu)	FOXI3 (P291L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2651108	NM_001135649.3(FOXI3):c.483G>T (p.Ala161=)	FOXI3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2057304	NM_001135649.3(FOXI3):c.438G>A (p.Pro146=)	FOXI3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1054456	NM_001135649.3(FOXI3):c.337GCGCCCGCC[3] (p.113APA[3])	FOXI3	Microsatellite (inframe_insertion)	not provided	GLikely benign
Select item 932705	NM_001135649.3(FOXI3):c.308del (p.Gly103fs)	FOXI3 (G103fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 1062261	NM_001135649.3(FOXI3):c.148G>C (p.Ala50Pro)	FOXI3 (A50P)	Single nucleotide variant (missense variant)	FOXI3-related condition +1 more	GBenign/Likely benign
Select item 1176758	GRCh37/hg19 2p11.2(chr2:88007281-90260248)x1	SMYD1, SPMIP9 +8 more	Copy number loss	not provided	GPathogenic

ClinVar