Colon Cancer: Gene >> KCNK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26728480:26728480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773773071
CDS Mutation	c.1097C>T
AA Mutation	p.Ala366Val(p.A366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26728003:26728003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620C>T
AA Mutation	p.Ala207Val(p.A207V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26728417:26728417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763388281
CDS Mutation	c.1034C>T
AA Mutation	p.Ser345Leu(p.S345L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26727691:26727691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308C>T
AA Mutation	p.Thr103Met(p.T103M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26727739:26727739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356C>T
AA Mutation	p.Pro119Leu(p.P119L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26728279:26728279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896T>C
AA Mutation	p.Val299Ala(p.V299A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302909
Start	26692972:26692972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97C>T
AA Mutation	p.Pro33Ser(p.P33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302909
Start	26728421:26728421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302909
Start	26728316:26728316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372175509
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302909
Start	26728106:26728106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302909
Start	26728256:26728256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302909
Start	26728206:26728206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.827delG
AA Mutation	p.Gly276ValfsTer52(p.G276Vfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302909
Start	26727722:26727722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302909
Start	26728058:26728058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript