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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051739	NM_003977.4(AIP):c.-5G>A	AIP	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 824477	NM_003977.4(AIP):c.-3A>G	AIP	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798666	NM_003977.4(AIP):c.-2G>A	AIP	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 825361	NM_003977.4(AIP):c.4G>C (p.Ala2Pro)	AIP (A2P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3223620	NM_003977.4(AIP):c.5C>T (p.Ala2Val)	AIP (A2V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1750985	NM_003977.4(AIP):c.5C>G (p.Ala2Gly)	AIP (A2G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1626086	NM_003977.4(AIP):c.6G>A (p.Ala2=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 3279195	NM_003977.4(AIP):c.8A>G (p.Asp3Gly)	AIP (D3G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1768950	NM_003977.4(AIP):c.9T>C (p.Asp3=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1515671	NM_003977.4(AIP):c.10A>G (p.Ile4Val)	AIP (I4V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2094440	NM_003977.4(AIP):c.11T>C (p.Ile4Thr)	AIP (I4T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1154113	NM_003977.4(AIP):c.12C>A (p.Ile4=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 818845	NM_003977.4(AIP):c.12C>G (p.Ile4Met)	AIP (I4M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2566790	NM_003977.4(AIP):c.16G>T (p.Ala6Ser)	AIP (A6S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1780364	NM_003977.4(AIP):c.17C>T (p.Ala6Val)	AIP (A6V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1780355	NM_003977.4(AIP):c.17C>A (p.Ala6Glu)	AIP (A6E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1047798	NM_003977.4(AIP):c.23T>G (p.Leu8Arg)	AIP (L8R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1792209	NM_003977.4(AIP):c.24C>G (p.Leu8=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 388468	NM_003977.4(AIP):c.25C>T (p.Arg9Trp)	AIP (R9W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1794911	NM_003977.4(AIP):c.26G>T (p.Arg9Leu)	AIP (R9L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 485052	NM_003977.4(AIP):c.26G>A (p.Arg9Gln)	AIP (R9Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 1797430	NM_003977.4(AIP):c.28G>A (p.Glu10Lys)	AIP (E10K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1668461	NM_003977.4(AIP):c.30G>A (p.Glu10=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2566784	NM_003977.4(AIP):c.31G>T (p.Asp11Tyr)	AIP (D11Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1405325	NM_003977.4(AIP):c.36G>T (p.Gly12=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1102270	NM_003977.4(AIP):c.36G>C (p.Gly12=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 305723	NM_003977.4(AIP):c.36G>A (p.Gly12=)	AIP	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1486213	NM_003977.4(AIP):c.37A>G (p.Ile13Val)	AIP (I13V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1406802	NM_003977.4(AIP):c.38T>A (p.Ile13Asn)	AIP (I13N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 4886	NM_003977.4(AIP):c.40C>T (p.Gln14Ter)	AIP (Q14*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 824668	NM_003977.4(AIP):c.41A>C (p.Gln14Pro)	AIP (Q14P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1741780	NM_003977.4(AIP):c.45A>G (p.Lys15=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1446003	NM_003977.4(AIP):c.46C>T (p.Arg16Cys)	AIP (R16C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 41184	NM_003977.4(AIP):c.47G>A (p.Arg16His)	AIP (R16H)	Single nucleotide variant (missense variant)	Familial isolated pituitary adenoma +3 more	GConflicting classifications of pathogenicity
Select item 1743979	NM_003977.4(AIP):c.48T>C (p.Arg16=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 2780216	NM_003977.4(AIP):c.51G>C (p.Val17=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 825703	NM_003977.4(AIP):c.53T>C (p.Ile18Thr)	AIP (I18T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1369274	NM_003977.4(AIP):c.56A>G (p.Gln19Arg)	AIP (Q19R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1083285	NM_003977.4(AIP):c.57G>A (p.Gln19=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 3223623	NM_003977.4(AIP):c.62G>T (p.Gly21Val)	AIP (G21V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1752722	NM_003977.4(AIP):c.62G>A (p.Gly21Asp)	AIP (G21D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 963750	NM_003977.4(AIP):c.62G>C (p.Gly21Ala)	AIP (G21A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1128637	NM_003977.4(AIP):c.63C>T (p.Gly21=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1753891	NM_003977.4(AIP):c.64C>A (p.Arg22=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2131911	NM_003977.4(AIP):c.65G>A (p.Arg22Gln)	AIP (R22Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 305724	NM_003977.4(AIP):c.68G>A (p.Gly23Glu)	AIP (G23E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 826838	NM_003977.4(AIP):c.70G>C (p.Glu24Gln)	AIP (E24Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 485057	NM_003977.4(AIP):c.72G>C (p.Glu24Asp)	AIP (E24D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 954536	NM_003977.4(AIP):c.73C>T (p.Leu25Phe)	AIP (L25F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1759723	NM_003977.4(AIP):c.75C>A (p.Leu25=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2821483	NM_003977.4(AIP):c.77C>T (p.Pro26Leu)	AIP (P26L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1761135	NM_003977.4(AIP):c.78G>T (p.Pro26=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1541075	NM_003977.4(AIP):c.78G>A (p.Pro26=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 3279474	NM_003977.4(AIP):c.79G>A (p.Asp27Asn)	AIP (D27N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1063510	NM_003977.4(AIP):c.79G>C (p.Asp27His)	AIP (D27H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1761988	NM_003977.4(AIP):c.80A>C (p.Asp27Ala)	AIP (D27A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2452494	NM_003977.4(AIP):c.81C>A (p.Asp27Glu)	AIP (D27E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1762415	NM_003977.4(AIP):c.81C>T (p.Asp27=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2452485	NM_003977.4(AIP):c.82T>C (p.Phe28Leu)	AIP (F28L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1110711	NM_003977.4(AIP):c.84T>C (p.Phe28=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2586843	NM_003977.4(AIP):c.85C>A (p.Gln29Lys)	AIP (Q29K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1764001	NM_003977.4(AIP):c.85C>G (p.Gln29Glu)	AIP (Q29E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1764703	NM_003977.4(AIP):c.87A>G (p.Gln29=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 954484	NM_003977.4(AIP):c.88G>T (p.Asp30Tyr)	AIP (D30Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1117434	NM_003977.4(AIP):c.90T>C (p.Asp30=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1368619	NM_003977.4(AIP):c.92G>C (p.Gly31Ala)	AIP (G31A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 864069	NM_003977.4(AIP):c.93G>T (p.Gly31=)	AIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 485068	NM_003977.4(AIP):c.93G>A (p.Gly31=)	AIP	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1767523	NM_003977.4(AIP):c.95C>T (p.Thr32Ile)	AIP (T32I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1767515	NM_003977.4(AIP):c.95C>A (p.Thr32Asn)	AIP (T32N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 859012	NM_003977.4(AIP):c.97A>G (p.Lys33Glu)	AIP (K33E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2562328	NM_003977.4(AIP):c.98A>G (p.Lys33Arg)	AIP (K33R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1768534	NM_003977.4(AIP):c.98A>C (p.Lys33Thr)	AIP (K33T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2954776	NM_003977.4(AIP):c.100-5C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1470153	NM_003977.4(AIP):c.100-4del	AIP, LOC130006206	Deletion (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2566786	NM_003977.4(AIP):c.100-3C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822003	NM_003977.4(AIP):c.100G>T (p.Ala34Ser)	AIP, LOC130006206 (A34S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 822001	NM_003977.4(AIP):c.100G>A (p.Ala34Thr)	AIP, LOC130006206 (A34T)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 485058	NM_003977.4(AIP):c.104C>T (p.Thr35Met)	AIP, LOC130006206 (T35M)	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GUncertain significance
Select item 1673800	NM_003977.4(AIP):c.105G>T (p.Thr35=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 818316	NM_003977.4(AIP):c.105G>A (p.Thr35=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2481055	NM_003977.4(AIP):c.106T>G (p.Phe36Val)	AIP, LOC130006206 (F36V)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822137	NM_003977.4(AIP):c.108C>T (p.Phe36=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GLikely benign
Select item 1728034	NM_003977.4(AIP):c.112T>C (p.Tyr38His)	AIP, LOC130006206 (Y38H)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1736248	NM_003977.4(AIP):c.115C>A (p.Arg39=)	LOC130006206, AIP	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1001466	NM_003977.4(AIP):c.115C>G (p.Arg39Gly)	AIP, LOC130006206 (R39G)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 861039	NM_003977.4(AIP):c.115C>T (p.Arg39Trp)	AIP, LOC130006206 (R39W)	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GUncertain significance
Select item 818481	NM_003977.4(AIP):c.116G>A (p.Arg39Gln)	LOC130006206, AIP (R39Q)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 818567	NM_003977.4(AIP):c.119C>T (p.Thr40Met)	AIP, LOC130006206 (T40M)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 818603	NM_003977.4(AIP):c.120G>A (p.Thr40=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GLikely benign
Select item 1543340	NM_003977.4(AIP):c.123G>A (p.Leu41=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2452495	NM_003977.4(AIP):c.124C>G (p.His42Asp)	AIP, LOC130006206 (H42D)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1769332	NM_003977.4(AIP):c.129T>C (p.Ser43=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 259204	NM_003977.4(AIP):c.132C>T (p.Asp44=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +3 more	GBenign
Select item 1040600	NM_003977.4(AIP):c.133G>A (p.Asp45Asn)	AIP, LOC130006206 (D45N)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1770561	NM_003977.4(AIP):c.134A>T (p.Asp45Val)	AIP, LOC130006206 (D45V)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 41162	NM_003977.4(AIP):c.135C>T (p.Asp45=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 819007	NM_003977.4(AIP):c.136G>A (p.Glu46Lys)	AIP, LOC130006206 (E46K)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GUncertain significance
Select item 1463124	NM_003977.4(AIP):c.138G>T (p.Glu46Asp)	AIP, LOC130006206 (E46D)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 41163	NM_003977.4(AIP):c.140_163del (p.Gly47_Arg54del)	AIP, LOC130006206	Deletion (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance

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