"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GOLM1"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2659287	NM_016548.4(GOLM1):c.825C>T (p.Gly275=)	GOLM1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659288	NM_016548.4(GOLM1):c.399G>C (p.Arg133Ser)	GOLM1 (R133S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 727548	NM_016548.4(GOLM1):c.105G>A (p.Ala35=)	GOLM1, LOC126860666	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign

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