"Ambry Genetics"[submitter] AND "PPM1B"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217318	NM_002706.6(PPM1B):c.220C>T (p.His74Tyr)	PPM1B (H74Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603986	NM_002706.6(PPM1B):c.413T>C (p.Met138Thr)	PPM1B (M138T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217319	NM_002706.6(PPM1B):c.433T>C (p.Tyr145His)	PPM1B (Y145H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299632	NM_002706.6(PPM1B):c.458G>A (p.Arg153His)	PPM1B (R153H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341838	NM_002706.6(PPM1B):c.470A>G (p.Tyr157Cys)	PPM1B (Y157C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301198	NM_002706.6(PPM1B):c.478G>A (p.Gly160Arg)	PPM1B (G160R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 810944	NM_002706.6(PPM1B):c.481C>G (p.Gln161Glu)	PPM1B (Q161E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217321	NM_002706.6(PPM1B):c.494C>T (p.Ser165Phe)	PPM1B (S165F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593093	NM_002706.6(PPM1B):c.532G>A (p.Glu178Lys)	PPM1B (E178K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217322	NM_002706.6(PPM1B):c.568C>G (p.Gln190Glu)	PPM1B (Q190E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607314	NM_002706.6(PPM1B):c.601G>A (p.Ala201Thr)	PPM1B (A201T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322513	NM_002706.6(PPM1B):c.809A>G (p.Asn270Ser)	PPM1B (N270S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209135	NM_002706.6(PPM1B):c.818A>G (p.Asn273Ser)	PPM1B (N273S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291684	NM_002706.6(PPM1B):c.831C>G (p.Asp277Glu)	PPM1B (D277E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217323	NM_002706.6(PPM1B):c.949G>C (p.Glu317Gln)	PPM1B (E30Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222139	NM_002706.6(PPM1B):c.955C>T (p.Arg319Trp)	PPM1B (R32W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217324	NM_002706.6(PPM1B):c.976A>G (p.Lys326Glu)	PPM1B (K326E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217325	NM_002706.6(PPM1B):c.996G>A (p.Met332Ile)	PPM1B (M45I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217315	NM_002706.6(PPM1B):c.1018C>T (p.Arg340Cys)	PPM1B (R340C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401489	NM_002706.6(PPM1B):c.1127G>A (p.Ser376Asn)	PPM1B (S376N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2476950	NM_002706.6(PPM1B):c.1194A>T (p.Gln398His)	PPM1B (Q111H +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3217316	NM_002706.6(PPM1B):c.1222C>G (p.Arg408Gly)	PPM1B (R121G +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3217317	NM_002706.6(PPM1B):c.1249A>G (p.Ser417Gly)	PPM1B (S417G +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2278870	NM_002706.6(PPM1B):c.1397C>G (p.Ser466Cys)	PPM1B (S466C +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign

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Items: 24