Colon Cancer: Gene >> SMTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31099751:31099751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747848868
CDS Mutation	c.2458G>A
AA Mutation	p.Asp820Asn(p.D820N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31087998:31087998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776743466
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Cys(p.R29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31099893:31099893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538229101
CDS Mutation	c.2600C>T
AA Mutation	p.Ala867Val(p.A867V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31096739:31096739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868G>A
AA Mutation	p.Arg623Gln(p.R623Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31099839:31099839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2546G>T
AA Mutation	p.Gly849Val(p.G849V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31089734:31089734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507G>T
AA Mutation	p.Glu169Asp(p.E169D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31091015:31091015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749629071
CDS Mutation	c.992G>A
AA Mutation	p.Arg331Gln(p.R331Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31091692:31091692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748870006
CDS Mutation	c.1477C>T
AA Mutation	p.Arg493Trp(p.R493W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31095439:31095439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1769G>T
AA Mutation	p.Gly590Val(p.G590V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31099108:31099108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2380G>A
AA Mutation	p.Gly794Arg(p.G794R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31096888:31096888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771689259
CDS Mutation	c.2017G>A
AA Mutation	p.Val673Ile(p.V673I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31088017:31088017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>C
AA Mutation	p.Arg35Pro(p.R35P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000347557
Start	31099072:31099072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2344G>C
AA Mutation	p.Gly782Arg(p.G782R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347557
Start	31090980:31090980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766142298
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347557
Start	31088018:31088018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347557
Start	31088900:31088900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141930003
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31089936:31089936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747405143
CDS Mutation	c.714delC
AA Mutation	p.Ser239AlafsTer118(p.S239Afs*118)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31091383:31091383(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1364delG
AA Mutation	p.Gly455AlafsTer3(p.G455Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31090967:31090967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.949delC
AA Mutation	p.Ala318ProfsTer39(p.A318Pfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31091813:31091813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778461809
CDS Mutation	c.1605delC
AA Mutation	p.Ser536ValfsTer33(p.S536Vfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000347557
Start	31090822:31090822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762131666
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Ter(p.R294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31090966:31090967(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.949dupC
AA Mutation	p.Leu317ProfsTer24(p.L317Pfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31091812:31091813(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758895137
CDS Mutation	c.1605dupC
AA Mutation	p.Ser536GlnfsTer2(p.S536Qfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000347557
Start	31099792:31099794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2501_2503delTCT
AA Mutation	p.Phe834del(p.F834del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SMTN

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347557
Start	31089936:31089936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747405143
CDS Mutation	c.714delC
AA Mutation	p.Ser239AlafsTer118(p.S239Afs*118)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript