Colon Cancer: Gene >> MAEL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	167021758:167021758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1208C>T
AA Mutation	p.Ser403Phe(p.S403F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	167017951:167017951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Cys(p.R345C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	167004261:167004261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605T>G
AA Mutation	p.Phe202Cys(p.F202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	167021125:167021125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082C>A
AA Mutation	p.Ser361Tyr(p.S361Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	167021715:167021715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202037854
CDS Mutation	c.1165C>T
AA Mutation	p.Arg389Trp(p.R389W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	166989419:166989419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Trp(p.R23W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	167004246:167004246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590A>G
AA Mutation	p.Gln197Arg(p.Q197R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367872
Start	166989391:166989391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>A
AA Mutation	p.Phe13Leu(p.F13L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367872
Start	166989382:166989382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000367872
Start	167005351:167005351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Ter(p.R267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367872
Start	166992707:166992708(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.353dupT
AA Mutation	p.Leu118PhefsTer5(p.L118Ffs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAEL

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000367872
Start	167005351:167005351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Ter(p.R267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367872
Start	167021146:167021147(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1106dupA
AA Mutation	p.Asn369LysfsTer6(p.N369Kfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript