Colon Cancer: Gene >> HLCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36936904:36936904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373411061
CDS Mutation	c.541G>A
AA Mutation	p.Glu181Lys(p.E181K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36930346:36930346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084G>A
AA Mutation	p.Glu362Lys(p.E362K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36897049:36897049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262G>T
AA Mutation	p.Arg421Ile(p.R421I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36754281:36754281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2146A>T
AA Mutation	p.Met716Leu(p.M716L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36936898:36936898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150431185
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Trp(p.R183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36767258:36767258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1479G>T
AA Mutation	p.Met493Ile(p.M493I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36936526:36936526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.919C>A
AA Mutation	p.Leu307Met(p.L307M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336648
Start	36936662:36936662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000336648
Start	36930397:36930397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033C>T
AA Mutation	p.Gln345Ter(p.Q345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HLCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36896993:36896993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>A
AA Mutation	p.Val440Met(p.V440M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336648
Start	36930346:36930346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084G>A
AA Mutation	p.Glu362Lys(p.E362K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript