"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TBC1D9B"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656141	NM_015043.4(TBC1D9B):c.2420G>A (p.Arg807Gln)	TBC1D9B (R807Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2656142	NM_015043.4(TBC1D9B):c.1803G>A (p.Ser601=)	LOC126807627, TBC1D9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656143	NM_015043.4(TBC1D9B):c.1503G>A (p.Thr501=)	TBC1D9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656144	NM_015043.4(TBC1D9B):c.1467C>T (p.Tyr489=)	TBC1D9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656145	NM_015043.4(TBC1D9B):c.949C>T (p.Leu317=)	TBC1D9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656146	NM_015043.4(TBC1D9B):c.686C>G (p.Ser229Cys)	TBC1D9B (S229C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656147	NM_015043.4(TBC1D9B):c.423G>A (p.Glu141=)	TBC1D9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar