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Gene: MLH3 & Disease: HNPCC7, 1799 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
161297	MLH3	c.4180G>A	p.Ala1394Thr (p.A1394T)	NM_001040108.2 M	SNV	VUS	1 +	5
5562	MLH3	c.4351G>A	p.Glu1451Lys (p.E1451K)	NM_001040108.2 M	SNV	LB	1 +	5
161297	MLH3	c.4108G>A	p.Ala1370Thr (p.A1370T)	NM_014381.3	SNV	VUS	1 +	5
5562	MLH3	c.4279G>A	p.Glu1427Lys (p.E1427K)	NM_014381.3	SNV	LB	1 +	5
5558	MLH3	c.70C>G	p.Gln24Glu (p.Q24E)	NM_001040108.2 M	SNV	VUS	1 +	4
5561	MLH3	c.2221G>T	p.Val741Phe (p.V741F)	NM_001040108.2 M	SNV	P	2 +	4
5564	MLH3	c.3826T>C	p.Trp1276Arg (p.W1276R)	NM_001040108.2 M	SNV	P	1 +	4
5558	MLH3	c.70C>G	p.Gln24Glu (p.Q24E)	NM_014381.3	SNV	VUS	1 +	4
5561	MLH3	c.2221G>T	p.Val741Phe (p.V741F)	NM_014381.3	SNV	P	2 +	4
5564	MLH3	c.3754T>C	p.Trp1252Arg (p.W1252R)	NM_014381.3	SNV	P	1 +	4
5563	MLH3	c.885del	p.His296fs (p.H296fs)	NM_001040108.2 M	Del	P	2 +	3
1133047	MLH3	c.1168T>A	p.Phe390Ile (p.F390I)	NM_001040108.2 M	SNV	LB	1 +	3
5560	MLH3	c.1870G>C	p.Glu624Gln (p.E624Q)	NM_001040108.2 M	SNV	LB	1 +	3
478032	MLH3	c.3020A>G	p.Asn1007Ser (p.N1007S)	NM_001040108.2 M	SNV	LB	1 +	3
314375	MLH3	c.3440A>T	p.Asn1147Ile (p.N1147I)	NM_001040108.2 M	SNV	LB	2 +	3
5563	MLH3	c.885del	p.His296fs (p.H296fs)	NM_014381.3	Del	P	2 +	3
1133047	MLH3	c.1168T>A	p.Phe390Ile (p.F390I)	NM_014381.3	SNV	LB	1 +	3
5560	MLH3	c.1870G>C	p.Glu624Gln (p.E624Q)	NM_014381.3	SNV	LB	1 +	3
478032	MLH3	c.3020A>G	p.Asn1007Ser (p.N1007S)	NM_014381.3	SNV	LB	1 +	3
314375	MLH3	c.3440A>T	p.Asn1147Ile (p.N1147I)	NM_014381.3	SNV	LB	2 +	3

1799 Results, 20 per Page

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