"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC1010599 - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2660892	NM_001323075.3(LOC101059915):c.597C>T (p.Gly199=)	LOC101059915	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660893	NM_001323075.3(LOC101059915):c.703G>A (p.Gly235Arg)	LOC101059915 (G235R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2660894	NM_001323075.3(LOC101059915):c.1068T>C (p.Ala356=)	LOC101059915, LOC126863278	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660895	NM_001323075.3(LOC101059915):c.1077G>A (p.Pro359=)	LOC101059915, LOC126863278	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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