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Mutation Direct

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Gene: AFF3 & Disease: KINS, 40 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
430951	AFF3	c.697G>A	p.Ala233Thr (p.A233T)	NM_001386135.1 M	SNV	P	1 +	2
	AFF3	c.772G>A	p.Ala258Thr (p.A258T)	NM_001025108.2	SNV	P	1 +	2
	AFF3	c.697G>A	p.Ala233Thr (p.A233T)	NM_002285.3	SNV	P	1 +	2
2479235	AFF3	c.664T>A	p.Ser222Thr (p.S222T)	NM_001386135.1 M	SNV	VUS	1 +	1
1077078	AFF3	c.692C>T	p.Pro231Leu (p.P231L)	NM_001386135.1 M	SNV	P	1 +	1
1077077	AFF3	c.691C>T	p.Pro231Ser (p.P231S)	NM_001386135.1 M	SNV	P	1 +	1
1338773	AFF3	c.692_693delinsGA	p.Pro231Arg (p.P231R)	NM_001386135.1 M	Indel	P	1 +	1
1077075	AFF3	c.697G>T	p.Ala233Ser (p.A233S)	NM_001386135.1 M	SNV	P	1 +	1
1077079	AFF3	c.704T>G	p.Val235Gly (p.V235G)	NM_001386135.1 M	SNV	P	1 +	1
1709819	AFF3	c.736G>C	p.Asp246His (p.D246H)	NM_001386135.1 M	SNV	VUS	1 +	1
1077076	AFF3	c.698C>T	p.Ala233Val (p.A233V)	NM_001386135.1 M	SNV	P	1 +	1
2441719	AFF3	c.1108C>T	p.Leu370Phe (p.L370F)	NM_001386135.1 M	SNV	VUS	1 +	1
2438910	AFF3	c.1518C>A	p.Asp506Glu (p.D506E)	NM_001386135.1 M	SNV	VUS	1 +	1
2444285	AFF3	c.1548del	p.Ser517fs (p.S517fs)	NM_001386135.1 M	Del	LP	1 +	1
2479235	AFF3	c.739T>A	p.Ser247Thr (p.S247T)	NM_001025108.2	SNV	VUS	1 +	1
2479235	AFF3	c.664T>A	p.Ser222Thr (p.S222T)	NM_002285.3	SNV	VUS	1 +	1
1077078	AFF3	c.767C>T	p.Pro256Leu (p.P256L)	NM_001025108.2	SNV	P	1 +	1
1077078	AFF3	c.692C>T	p.Pro231Leu (p.P231L)	NM_002285.3	SNV	P	1 +	1
1077077	AFF3	c.766C>T	p.Pro256Ser (p.P256S)	NM_001025108.2	SNV	P	1 +	1
1077077	AFF3	c.691C>T	p.Pro231Ser (p.P231S)	NM_002285.3	SNV	P	1 +	1

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