Colon Cancer: Gene >> GML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142846617:142846617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404G>T
AA Mutation	p.Gly135Val(p.G135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142840502:142840502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200642476
CDS Mutation	c.65G>A
AA Mutation	p.Arg22His(p.R22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142846626:142846626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Lys(p.R138K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142841190:142841190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768613353
CDS Mutation	c.146C>T
AA Mutation	p.Pro49Leu(p.P49L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142841142:142841142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98A>T
AA Mutation	p.Asp33Val(p.D33V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142841154:142841154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110T>C
AA Mutation	p.Ile37Thr(p.I37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142846615:142846615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402A>C
AA Mutation	p.Glu134Asp(p.E134D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142846643:142846643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430C>A
AA Mutation	p.Leu144Met(p.L144M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220940
Start	142841225:142841225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150041552
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Cys(p.R61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142846635:142846635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422T>C
AA Mutation	p.Val141Ala(p.V141A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220940
Start	142846600:142846600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220940
Start	142846636:142846636(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.423delA
AA Mutation	p.Ser142GlnfsTer5(p.S142Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000220940
Start	142846589:142846589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376G>T
AA Mutation	p.Glu126Ter(p.E126*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220940
Start	142846572:142846572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359G>T
AA Mutation	p.Arg120Met(p.R120M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript