"MLLT10-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055784	NM_001195626.3(MLLT10):c.195G>A (p.Pro65=)	MLLT10	Single nucleotide variant (synonymous variant +2 more)	MLLT10-related disorder	GBenign
Select item 3038919	NM_001195626.3(MLLT10):c.240+17954A>T	MLLT10 (D155V)	Single nucleotide variant (3 prime UTR variant +2 more)	MLLT10-related disorder	GBenign
Select item 3042783	NM_001195626.3(MLLT10):c.297T>C (p.Gly99=)	MLLT10	Single nucleotide variant (synonymous variant +2 more)	MLLT10-related disorder	GLikely benign
Select item 3050487	NM_001195626.3(MLLT10):c.406-11_406-10del	MLLT10	Deletion (intron variant)	MLLT10-related disorder	GBenign
Select item 3037162	NM_001195626.3(MLLT10):c.705T>C (p.Tyr235=)	MLLT10	Single nucleotide variant (synonymous variant +2 more)	MLLT10-related disorder	GLikely benign
Select item 3039949	NM_001195626.3(MLLT10):c.1052-14_1052-10del	MLLT10	Deletion (intron variant)	MLLT10-related disorder	GLikely benign
Select item 3050599	NM_001195626.3(MLLT10):c.1200T>C (p.His400=)	MLLT10	Single nucleotide variant (synonymous variant +1 more)	MLLT10-related disorder	GLikely benign
Select item 3040443	NM_001195626.3(MLLT10):c.1622-4A>G	MLLT10	Single nucleotide variant (intron variant)	MLLT10-related disorder	GLikely benign
Select item 3034963	NM_001195626.3(MLLT10):c.1897T>A (p.Ser633Thr)	MLLT10 (S388T +2 more)	Single nucleotide variant (missense variant +1 more)	MLLT10-related disorder	GLikely benign
Select item 3055555	NM_001195626.3(MLLT10):c.1991-4A>G	MLLT10	Single nucleotide variant (intron variant)	MLLT10-related disorder	GLikely benign
Select item 3048925	NM_001195626.3(MLLT10):c.2090G>A (p.Arg697His)	MLLT10 (R452H +2 more)	Single nucleotide variant (missense variant +1 more)	MLLT10-related disorder	GLikely benign
Select item 3055376	NM_001195626.3(MLLT10):c.2943A>G (p.Gln981=)	MLLT10	Single nucleotide variant (synonymous variant +1 more)	MLLT10-related disorder	GLikely benign