"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DRAXIN"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2638237	NM_001127325.2(MAD2L2):c.-13+3286G>A	DRAXIN, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2638238	NM_198545.4(DRAXIN):c.178C>T (p.Arg60Trp)	DRAXIN (R60W)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2638239	NM_198545.4(DRAXIN):c.937+6T>A	DRAXIN	Single nucleotide variant (intron variant)	not provided	GLikely benign

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