Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KCNK15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372861
Start	44750540:44750540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695T>C
AA Mutation	p.Leu232Pro(p.L232P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372861
Start	44750201:44750201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356C>T
AA Mutation	p.Pro119Leu(p.P119L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372861
Start	44750140:44750140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295G>A
AA Mutation	p.Ala99Thr(p.A99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372861
Start	44750244:44750244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372861
Start	44746165:44746165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372861
Start	44750247:44750247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372861
Start	44750562:44750562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372861
Start	44750475:44750475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372861
Start	44750246:44750246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401C>T
AA Mutation	p.Ala134Val(p.A134V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript