"Ambry Genetics"[submitter] AND "MYB"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2236319	NM_001130173.2(MYB):c.12A>C (p.Arg4Ser)	MYB (R4S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2458957	NM_001130173.2(MYB):c.832G>A (p.Ala278Thr)	MYB (A278T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2601420	NM_001130173.2(MYB):c.966C>G (p.Cys322Trp)	MYB (C287W +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2544406	NM_001130173.2(MYB):c.1242C>A (p.Phe414Leu)	MYB (F414L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2206745	NM_001130173.2(MYB):c.1303C>A (p.Gln435Lys)	MYB (Q435K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2481588	NM_001130173.2(MYB):c.1472C>A (p.Ala491Asp)	MYB (A488D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2411419	NM_001130173.2(MYB):c.1631C>A (p.Pro544His)	MYB (P420H +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2289108	NM_001130173.2(MYB):c.1677C>A (p.Asp559Glu)	MYB (D353E +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2310693	NM_001130173.2(MYB):c.1778A>G (p.His593Arg)	MYB (H387R +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2476198	NM_001130173.2(MYB):c.1937A>G (p.Lys646Arg)	MYB (K525R +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2606435	NM_001130173.2(MYB):c.2031C>A (p.Phe677Leu)	MYB (F471L +6 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2622055	NM_001130173.2(MYB):c.2098T>A (p.Ser700Thr)	MYB (S542T +7 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2516951	NM_001130173.2(MYB):c.2201G>A (p.Cys734Tyr)	MYB (C718Y +7 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2473979	NM_001130173.2(MYB):c.2234G>C (p.Ser745Thr)	MYB (S621T +7 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance