MLLT1[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2649131	NM_005934.4(MLLT1):c.1643G>A (p.Arg548His)	MLLT1 (R548H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2543495	NM_005934.4(MLLT1):c.1630G>A (p.Glu544Lys)	MLLT1 (E544K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204339	NM_005934.4(MLLT1):c.1460A>G (p.Lys487Arg)	MLLT1 (K487R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204309	NM_005934.4(MLLT1):c.1426C>T (p.Pro476Ser)	MLLT1 (P476S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 242890	NM_005934.4(MLLT1):c.1418G>A (p.Arg473Gln)	MLLT1 (R473Q)	Single nucleotide variant (missense variant)	Hypertelorism +6 more	GLikely pathogenic
Select item 2486738	NM_005934.4(MLLT1):c.1364G>A (p.Arg455His)	MLLT1 (R455H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359068	NM_005934.4(MLLT1):c.1345G>A (p.Asp449Asn)	MLLT1 (D449N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204201	NM_005934.4(MLLT1):c.1103A>C (p.Lys368Thr)	MLLT1 (K368T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247363	NM_005934.4(MLLT1):c.1057G>A (p.Ala353Thr)	MLLT1 (A353T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204587	NM_005934.4(MLLT1):c.974C>T (p.Ser325Leu)	MLLT1 (S325L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372546	NM_005934.4(MLLT1):c.938G>C (p.Gly313Ala)	MLLT1 (G313A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610859	NM_005934.4(MLLT1):c.925C>T (p.Arg309Trp)	MLLT1 (R309W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620369	NM_005934.4(MLLT1):c.886A>G (p.Ser296Gly)	MLLT1 (S296G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295189	NM_005934.4(MLLT1):c.868G>A (p.Ala290Thr)	MLLT1 (A290T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204465	NM_005934.4(MLLT1):c.860C>T (p.Pro287Leu)	MLLT1 (P287L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295190	NM_005934.4(MLLT1):c.794G>T (p.Ser265Ile)	MLLT1 (S265I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 718642	NM_005934.4(MLLT1):c.689C>T (p.Ser230Leu)	MLLT1 (S230L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3204433	NM_005934.4(MLLT1):c.554A>G (p.Asn185Ser)	MLLT1 (N185S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2560087	NM_005934.4(MLLT1):c.469G>A (p.Asp157Asn)	MLLT1 (D157N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620930	NM_005934.4(MLLT1):c.449C>A (p.Thr150Lys)	MLLT1 (T150K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20