Colon Cancer: Gene >> LUM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91104239:91104239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144708376
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Cys(p.R315C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108931:91108931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200635075
CDS Mutation	c.49A>G
AA Mutation	p.Ser17Gly(p.S17G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108196:91108196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784T>C
AA Mutation	p.Ser262Pro(p.S262P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108834:91108834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146G>A
AA Mutation	p.Ser49Asn(p.S49N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91104193:91104193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108819:91108819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>G
AA Mutation	p.Asp54Gly(p.D54G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108469:91108469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511C>A
AA Mutation	p.Leu171Met(p.L171M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108730:91108730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250A>G
AA Mutation	p.Lys84Glu(p.K84E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108262:91108262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603717
CDS Mutation	c.718G>A
AA Mutation	p.Glu240Lys(p.E240K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266718
Start	91104297:91104297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266718
Start	91108422:91108422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144214151
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266718
Start	91108472:91108472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000266718
Start	91108463:91108463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>T
AA Mutation	p.Glu173Ter(p.E173*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000266718
Start	91109001:91109001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-21-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LUM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108405:91108405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575G>C
AA Mutation	p.Ser192Thr(p.S192T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108262:91108262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603717
CDS Mutation	c.718G>A
AA Mutation	p.Glu240Lys(p.E240K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266718
Start	91108405:91108405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575G>A
AA Mutation	p.Ser192Asn(p.S192N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript