Colon Cancer: Gene >> KCNN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17988436:17988436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1081G>A
AA Mutation	p.Val361Met(p.V361M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17974201:17974201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17973897:17973897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9C>G
AA Mutation	p.Ser3Arg(p.S3R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17974028:17974028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17981919:17981919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17982057:17982057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847G>A
AA Mutation	p.Gly283Ser(p.G283S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17993495:17993495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773288101
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438Gln(p.R438Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17982021:17982021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Cys(p.R271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17974225:17974225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337T>C
AA Mutation	p.Phe113Leu(p.F113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222249
Start	17973915:17973915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77030907
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222249
Start	17981759:17981759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772127918
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222249
Start	17981972:17981972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774495537
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222249
Start	17982026:17982026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753480253
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17982114:17982114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774227733
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Cys(p.R302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17981821:17981821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611A>G
AA Mutation	p.His204Arg(p.H204R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222249
Start	17989819:17989819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274G>A
AA Mutation	p.Arg425His(p.R425H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript