Colon Cancer: Gene >> AACS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125103015:125103015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552840406
CDS Mutation	c.701A>C
AA Mutation	p.Lys234Thr(p.K234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125114534:125114534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>T
AA Mutation	p.Asp325Tyr(p.D325Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125103068:125103068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754A>G
AA Mutation	p.Lys252Glu(p.K252E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125073921:125073921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179A>G
AA Mutation	p.Asp60Gly(p.D60G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125073934:125073934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192G>T
AA Mutation	p.Glu64Asp(p.E64D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125102749:125102749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641G>A
AA Mutation	p.Gly214Asp(p.G214D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125142140:125142140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1930G>A
AA Mutation	p.Ala644Thr(p.A644T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125134798:125134798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1624G>A
AA Mutation	p.Gly542Ser(p.G542S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125124961:125124961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752378439
CDS Mutation	c.1246G>T
AA Mutation	p.Ala416Ser(p.A416S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125102688:125102688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580G>A
AA Mutation	p.Asp194Asn(p.D194N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125142152:125142152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765733198
CDS Mutation	c.1942G>A
AA Mutation	p.Val648Met(p.V648M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316519
Start	125129342:125129342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781595318
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316519
Start	125073967:125073967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316519
Start	125118714:125118714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1075delC
AA Mutation	p.Leu359TrpfsTer15(p.L359Wfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AACS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125091515:125091515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Gly188Ser(p.G188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316519
Start	125107181:125107181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828C>G
AA Mutation	p.Phe276Leu(p.F276L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript