Colon Cancer: Gene >> MSH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80672257:80672257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806A>G
AA Mutation	p.Glu269Gly(p.E269G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80775711:80775711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2271G>T
AA Mutation	p.Lys757Asn(p.K757N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80665211:80665211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138381683
CDS Mutation	c.427G>A
AA Mutation	p.Asp143Asn(p.D143N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80875787:80875787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145769847
CDS Mutation	c.3339G>A
AA Mutation	p.Met1113Ile(p.M1113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80670265:80670265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762864714
CDS Mutation	c.748G>A
AA Mutation	p.Val250Met(p.V250M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80670263:80670263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746G>A
AA Mutation	p.Cys249Tyr(p.C249Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80778760:80778760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2359G>A
AA Mutation	p.Glu787Lys(p.E787K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80767947:80767947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911G>T
AA Mutation	p.Glu637Asp(p.E637D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265081
Start	80761657:80761657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265081
Start	80792766:80792766(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2582delA
AA Mutation	p.Asn861MetfsTer6(p.N861Mfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265081
Start	80864865:80864865(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3059delA
AA Mutation	p.Asn1020IlefsTer40(p.N1020Ifs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265081
Start	80864864:80864865(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3059dupA
AA Mutation	p.Asn1020LysfsTer17(p.N1020Kfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265081
Start	80768981:80768982(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2231_2232insCATATTCGAAGTTTAT
AA Mutation	p.Val745IlefsTer28(p.V745Ifs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MSH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80670291:80670291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774C>A
AA Mutation	p.Phe258Leu(p.F258L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80725547:80725547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435G>T
AA Mutation	p.Asp479Tyr(p.D479Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80665150:80665150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366G>T
AA Mutation	p.Lys122Asn(p.K122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265081
Start	80873231:80873231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3246T>G
AA Mutation	p.Ile1082Met(p.I1082M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript