Colon Cancer: Gene >> GEM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297596
Start	94252096:94252096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536G>A
AA Mutation	p.Arg179Gln(p.R179Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297596
Start	94260395:94260395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109C>A
AA Mutation	p.Pro37Thr(p.P37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297596
Start	94252043:94252043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187593880
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Trp(p.R197W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297596
Start	94253109:94253109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335A>T
AA Mutation	p.Asp112Val(p.D112V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297596
Start	94260193:94260193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311G>A
AA Mutation	p.Ser104Asn(p.S104N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297596
Start	94250382:94250382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297596
Start	94252137:94252137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571339649
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297596
Start	94250520:94250520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000297596
Start	94252118:94252118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Ter(p.R172*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000297596
Start	94260330:94260330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174G>A
AA Mutation	p.Trp58Ter(p.W58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GEM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297596
Start	94250477:94250477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749374110
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Trp(p.R242W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297596
Start	94253066:94253066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763307759
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297596
Start	94250425:94250426(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.775_776insT
AA Mutation	p.Lys259IlefsTer34(p.K259Ifs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript