Colon Cancer: Gene >> TGFBR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30672151:30672151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968T>C
AA Mutation	p.Leu323Pro(p.L323P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30644864:30644864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212G>A
AA Mutation	p.Cys71Tyr(p.C71Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30644884:30644884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>A
AA Mutation	p.Glu78Lys(p.E78K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30674186:30674186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336G>A
AA Mutation	p.Asp446Asn(p.D446N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30674172:30674172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322C>T
AA Mutation	p.Ser441Phe(p.S441F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30691478:30691478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104893815
CDS Mutation	c.1583G>A
AA Mutation	p.Arg528His(p.R528H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30691477:30691477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104893810
CDS Mutation	c.1582C>T
AA Mutation	p.Arg528Cys(p.R528C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295754
Start	30644754:30644754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753739611
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295754
Start	30672110:30672110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756625146
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295754
Start	30672167:30672167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193922666
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295754
Start	30644871:30644871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295754
Start	30672132:30672132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000295754
Start	30688476:30688476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489C>T
AA Mutation	p.Arg497Ter(p.R497*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000295754
Start	30671976:30671976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793C>T
AA Mutation	p.Gln265Ter(p.Q265*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295754
Start	30691458:30691459(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1564_1567dupGACC
AA Mutation	p.His523ArgfsTer19(p.H523Rfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000295754
Start	30671879:30671881(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.701_703delACA
AA Mutation	p.Asn234del(p.N234del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TGFBR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295754
Start	30671802:30671802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775640617
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Trp(p.R207W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript