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Gene: MSH3 & Disease: FAP4, 66 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
656200	MSH3	c.2041C>T	p.Pro681Ser (p.P681S)	NM_002439.5 M	SNV	LB	1 +	5
648498	MSH3	c.1341-1G>T	--	NM_002439.5 M	SNV	LP	1 +	4
653005	MSH3	c.1394A>G	p.Tyr465Cys (p.Y465C)	NM_002439.5 M	SNV	VUS	1 +	4
253325	MSH3	c.2319-1G>A	--	NM_002439.5 M	SNV	P	1 +	4
8738	MSH3	c.1148del	p.Lys383fs (p.K383fs)	NM_002439.5 M	Del	P	2 +	3
661178	MSH3	c.2655+1G>A	--	NM_002439.5 M	SNV	LP	1 +	3
785130	MSH3	c.1571A>C	p.Asn524Thr (p.N524T)	NM_002439.5 M	SNV	LB	1 +	3
253324	MSH3	c.2760del	p.Tyr921fs (p.Y921fs)	NM_002439.5 M	Del	P	1 +	3
1040708	MSH3	c.1028-1A>T	--	NM_002439.5 M	SNV	VUS	2 +	2
640523	MSH3	c.2336G>A	p.Arg779His (p.R779H)	NM_002439.5 M	SNV	VUS	1 +	2
649390	MSH3	c.2663C>G	p.Ser888Ter (p.S888X)	NM_002439.5 M	SNV	P	1 +	2
953546	MSH3	c.1764-2A>G	--	NM_002439.5 M	SNV	LP	1 +	2
1478255	MSH3	c.3130+1G>A	--	NM_002439.5 M	SNV	LP	1 +	2
938273	MSH3	c.2318+5del	--	NM_002439.5 M	Del	LP	1 +	2
864772	MSH3	c.1653+1G>A	--	NM_002439.5 M	SNV	LP	1 +	2
758451	MSH3	c.3181A>G	p.Arg1061Gly (p.R1061G)	NM_002439.5 M	SNV	LB	1 +	2
660399	MSH3	c.2044G>C	p.Val682Leu (p.V682L)	NM_002439.5 M	SNV	VUS	1 +	2
1709103	MSH3	c.763A>T	p.Lys255Ter (p.K255X)	NM_002439.5 M	SNV	P	1 +	2
1799405	MSH3	c.3064_3067del	p.Ser1022fs (p.S1022fs)	NM_002439.5 M	Del	P	1 +	2
644460	MSH3	c.1360C>T	p.Arg454Ter (p.R454X)	NM_002439.5 M	SNV	P	1 +	2

66 Results, 20 per Page

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