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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 29

	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)	not specified	GUncertain significance
Select item 3153005	NM_001130173.2(MYB):c.647A>G (p.Lys216Arg)	MYB (K216R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297153	NM_001130173.2(MYB):c.778C>G (p.Pro260Ala)	MYB (P260A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458957	NM_001130173.2(MYB):c.832G>A (p.Ala278Thr)	MYB (A278T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601420	NM_001130173.2(MYB):c.966C>G (p.Cys322Trp)	MYB (C287W +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 3152956	NM_001130173.2(MYB):c.1365G>A (p.Met455Ile)	MYB (M452I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 3152963	NM_001130173.2(MYB):c.1495A>C (p.Ile499Leu)	MYB (I483L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3152964	NM_001130173.2(MYB):c.1594A>G (p.Asn532Asp)	MYB (N376D +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152967	NM_001130173.2(MYB):c.1615T>C (p.Ser539Pro)	MYB (S418P +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 3152974	NM_001130173.2(MYB):c.1633C>G (p.Leu545Val)	MYB (L339V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297151	NM_001130173.2(MYB):c.1675G>C (p.Asp559His)	MYB (D403H +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 3297155	NM_001130173.2(MYB):c.1698G>C (p.Lys566Asn)	MYB (K360N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152978	NM_001130173.2(MYB):c.1705A>G (p.Thr569Ala)	MYB (T448A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152980	NM_001130173.2(MYB):c.1726A>G (p.Ile576Val)	MYB (I370V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152983	NM_001130173.2(MYB):c.1756A>G (p.Arg586Gly)	MYB (R465G +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 3152990	NM_001130173.2(MYB):c.1819A>T (p.Met607Leu)	MYB (M451L +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 3297152	NM_001130173.2(MYB):c.2156C>A (p.Ala719Glu)	MYB (A561E +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 3153001	NM_001130173.2(MYB):c.2227T>C (p.Ser743Pro)	MYB (S622P +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 29