Colon Cancer: Gene >> KCNJ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839330:128839330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971G>A
AA Mutation	p.Arg324His(p.R324H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128840057:128840057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244A>T
AA Mutation	p.Thr82Ser(p.T82S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839993:128839993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764778741
CDS Mutation	c.308C>T
AA Mutation	p.Ala103Val(p.A103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839331:128839331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760450195
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Cys(p.R324C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839325:128839325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775088508
CDS Mutation	c.976G>T
AA Mutation	p.Ala326Ser(p.A326S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839456:128839456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392664
Start	128839161:128839161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773891455
CDS Mutation	c.1140G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392664
Start	128840076:128840076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392664
Start	128839722:128839722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150487168
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000392664
Start	128840181:128840182(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.119_120insCCCAAG
AA Mutation	p.Ala40_Arg41insProArg(p.A40_R41insPR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNJ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128840159:128840159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142A>T
AA Mutation	p.Arg48Trp(p.R48W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128840124:128840124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177G>T
AA Mutation	p.Gln59His(p.Q59H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839747:128839747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554C>T
AA Mutation	p.Pro185Leu(p.P185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392664
Start	128839171:128839171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130A>C
AA Mutation	p.Asn377Thr(p.N377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript