Colon Cancer: Gene >> KCNK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139702733:139702733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260C>T
AA Mutation	p.Ala87Val(p.A87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618475:139618475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908G>A
AA Mutation	p.Arg303His(p.R303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618818:139618818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>A
AA Mutation	p.Ala189Thr(p.A189T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618776:139618776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765113254
CDS Mutation	c.607G>A
AA Mutation	p.Gly203Arg(p.G203R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618460:139618460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758730965
CDS Mutation	c.923G>A
AA Mutation	p.Gly308Asp(p.G308D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618455:139618455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753797613
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Cys(p.R310C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618274:139618274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781672892
CDS Mutation	c.1109G>A
AA Mutation	p.Arg370His(p.R370H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303015
Start	139618924:139618924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776045672
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303015
Start	139702927:139702927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773306121
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303015
Start	139618459:139618459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748355464
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303015
Start	139702915:139702915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303015
Start	139618819:139618819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303015
Start	139618519:139618519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760013455
CDS Mutation	c.864G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000303015
Start	139702901:139702901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92C>A
AA Mutation	p.Ser31Ter(p.S31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303015
Start	139618772:139618773(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.610dupG
AA Mutation	p.Asp204GlyfsTer21(p.D204Gfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303015
Start	139618973:139618973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758314044
CDS Mutation	c.410G>A
AA Mutation	p.Arg137His(p.R137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript