Colon Cancer: Gene >> GLP1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39085921:39085921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199796313
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Trp(p.R414W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39085939:39085939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258T>C
AA Mutation	p.Trp420Arg(p.W420R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39057525:39057525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>T
AA Mutation	p.Pro77Ser(p.P77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39056461:39056461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150253529
CDS Mutation	c.143G>A
AA Mutation	p.Arg48His(p.R48H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39056437:39056437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200849157
CDS Mutation	c.119G>A
AA Mutation	p.Arg40Gln(p.R40Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39072961:39072961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>C
AA Mutation	p.Trp203Cys(p.W203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39072962:39072962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610A>C
AA Mutation	p.Met204Leu(p.M204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373256
Start	39066235:39066235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000373256
Start	39079610:39079610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>T
AA Mutation	p.Glu364Ter(p.E364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GLP1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39073640:39073640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772199865
CDS Mutation	c.694C>T
AA Mutation	p.Leu232Phe(p.L232F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39072943:39072943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591G>T
AA Mutation	p.Lys197Asn(p.K197N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39056448:39056448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201675748
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Cys(p.R44C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373256
Start	39072944:39072944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592G>T
AA Mutation	p.Asp198Tyr(p.D198Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373256
Start	39066250:39066250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200564025
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373256
Start	39079562:39079562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript