Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KCNK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39191483:39191483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>A
AA Mutation	p.Asp303Asn(p.D303N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39229042:39229042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70G>A
AA Mutation	p.Glu24Lys(p.E24K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39191441:39191441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142417837
CDS Mutation	c.949G>A
AA Mutation	p.Gly317Arg(p.G317R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39191305:39191305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085T>C
AA Mutation	p.Leu362Pro(p.L362P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39191035:39191035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355G>T
AA Mutation	p.Gly452Val(p.G452V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39194318:39194318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485G>A
AA Mutation	p.Cys162Tyr(p.C162Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359534
Start	39194648:39194648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756396615
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359534
Start	39191097:39191097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144931567
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359534
Start	39229066:39229066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748059487
CDS Mutation	c.46C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359534
Start	39191274:39191275(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1115_1116insTGGA
AA Mutation	p.Asp373GlyfsTer3(p.D373Gfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39190940:39190940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539017498
CDS Mutation	c.1450G>A
AA Mutation	p.Glu484Lys(p.E484K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39191483:39191483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907G>T
AA Mutation	p.Asp303Tyr(p.D303Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359534
Start	39191356:39191356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034T>C
AA Mutation	p.Val345Ala(p.V345A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript