"Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan"[submitte - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1223921	NM_001323329.2(MAPK8):c.-49-77C>A	MAPK8	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1223363	NM_001323329.2(MAPK8):c.123-51A>C	MAPK8	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1260927	NM_001323329.2(MAPK8):c.253-80T>A	MAPK8	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1259128	NM_001323329.2(MAPK8):c.311+37A>G	MAPK8	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 2688159	NM_001323329.2(MAPK8):c.871+66G>A	MAPK8	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688199	NM_001323329.2(MAPK8):c.1060+91T>G	MAPK8	Single nucleotide variant (intron variant)	not specified	GBenign

ClinVar