Colon Cancer: Gene >> HAL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95976611:95976611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777581036
CDS Mutation	c.1750C>T
AA Mutation	p.Arg584Cys(p.R584C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95976673:95976673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688G>A
AA Mutation	p.Gly563Asp(p.G563D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95994115:95994115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386T>C
AA Mutation	p.Leu129Ser(p.L129S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95995769:95995769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780228604
CDS Mutation	c.142G>A
AA Mutation	p.Val48Met(p.V48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95986113:95986113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771145104
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Trp(p.R367W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95976659:95976659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765722855
CDS Mutation	c.1702C>T
AA Mutation	p.Arg568Cys(p.R568C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95995811:95995811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Cys(p.R34C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95976638:95976638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1723C>T
AA Mutation	p.Pro575Ser(p.P575S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95974338:95974338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1868A>G
AA Mutation	p.Tyr623Cys(p.Y623C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95995886:95995886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201646460
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Cys(p.R9C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95995745:95995745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Cys(p.R56C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261208
Start	95974364:95974364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1842A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261208
Start	95992783:95992783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261208
Start	95976462:95976462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137860207
CDS Mutation	c.1800C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261208
Start	95994947:95994947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261208
Start	95990486:95990486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.762T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000261208
Start	95987154:95987154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34457757
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Ter(p.R322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HAL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95980661:95980661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147706824
CDS Mutation	c.1414G>A
AA Mutation	p.Glu472Lys(p.E472K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261208
Start	95990507:95990507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.741G>T
AA Mutation	p.Glu247Asp(p.E247D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261208
Start	95980662:95980662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755913078
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript