Colon Cancer: Gene >> KCNK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215086647:215086647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326T>C
AA Mutation	p.Val109Ala(p.V109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215172163:215172163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803G>T
AA Mutation	p.Gly268Val(p.G268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215169253:215169253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530A>G
AA Mutation	p.Tyr177Cys(p.Y177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215235122:215235122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>T
AA Mutation	p.Ala420Ser(p.A420S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215172180:215172180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>T
AA Mutation	p.Ala274Ser(p.A274S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215234849:215234849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Ala329Thr(p.A329T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215169231:215169231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781364297
CDS Mutation	c.508G>A
AA Mutation	p.Gly170Ser(p.G170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215172156:215172156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796A>G
AA Mutation	p.Thr266Ala(p.T266A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000444842
Start	215234848:215234848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773024551
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000444842
Start	215086504:215086504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375389536
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000444842
Start	215169221:215169221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000444842
Start	215194960:215194960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149941939
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215086653:215086653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748830571
CDS Mutation	c.332C>T
AA Mutation	p.Ser111Leu(p.S111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000444842
Start	215234879:215234879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015G>A
AA Mutation	p.Glu339Lys(p.E339K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000444842
Start	215234878:215234878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751828549
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000444842
Start	215169281:215169281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000444842
Start	215169225:215169225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502G>T
AA Mutation	p.Glu168Ter(p.E168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript