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Gene: INS-IGF2 & Disease: MODY10, 29 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
617648	INS-IGF2	c.187+890C>G	--	NM_001042376.3	SNV	LP	2 +	8
68727	INS-IGF2	c.17G>A	p.Arg6His (p.R6H)	NM_001042376.3	SNV	VUS	1 +	6
13391	INS-IGF2	c.137G>A	p.Arg46Gln (p.R46Q)	NM_001042376.3	SNV	P	1 +	5
36400	INS-IGF2	c.187+772C>T	--	NM_001042376.3	SNV	LB	6 +	4
880304	INS-IGF2	c.72C>A	p.Ala24= (p.A24=)	NM_001042376.3	SNV	LB	2 +	4
129279	INS-IGF2	c.187+778G>A	--	NM_001042376.3	SNV	LB	6 +	4
304049	INS-IGF2	c.187+975C>T	--	NM_001042376.3	SNV	B	2 +	4
304050	INS-IGF2	c.187+961G>A	--	NM_001042376.3	SNV	LB	2 +	4
304052	INS-IGF2	c.187+935C>T	--	NM_001042376.3	SNV	LB	2 +	4
304053	INS-IGF2	c.187+785C>A	--	NM_001042376.3	SNV	VUS	2 +	4
304058	INS-IGF2	c.25C>T	p.Pro9Ser (p.P9S)	NM_001042376.3	SNV	VUS	5 +	4
304061	INS-IGF2	c.-18+3C>G	--	NM_001042376.3	SNV	B	2 +	4
1162205	INS-IGF2	c.115C>T	p.Leu39Phe (p.L39F)	NM_001042376.3	SNV	LP	2 +	4
255531	INS-IGF2	c.187+942C>T	--	NM_001042376.3	SNV	LB	3 +	2
13390	INS-IGF2	c.16C>T	p.Arg6Cys (p.R6C)	NM_001042376.3	SNV	P	1 +	2
1455986	INS-IGF2	c.1A>G	p.Met1Val (p.M1V)	NM_001042376.3	SNV	P	4 +	2
931331	INS-IGF2	c.155C>T	p.Pro52Leu (p.P52L)	NM_001042376.3	SNV	P	1 +	1
255532	INS-IGF2	c.187+11T>C	--	NM_001042376.3	SNV	LB	7 +	1
36399	INS-IGF2	c.-9C>T	--	NM_001042376.3	SNV	LB	4 +	1
730224	INS-IGF2	c.67G>A	p.Ala23Thr (p.A23T)	NM_001042376.3	SNV	LB	4 +	1

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