Colon Cancer: Gene >> KCNN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154725965:154725965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697C>T
AA Mutation	p.Ala566Val(p.A566V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154869382:154869382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Trp(p.R195W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154772230:154772230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771961515
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398Gln(p.R398Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154869334:154869334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631T>C
AA Mutation	p.Phe211Leu(p.F211L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154772372:154772372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051G>A
AA Mutation	p.Ala351Thr(p.A351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154772360:154772360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769288919
CDS Mutation	c.1063C>T
AA Mutation	p.Arg355Trp(p.R355W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154725954:154725954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708G>A
AA Mutation	p.Val570Ile(p.V570I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154707986:154707986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2231G>A
AA Mutation	p.Ser744Asn(p.S744N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154772271:154772271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1152C>A
AA Mutation	p.Phe384Leu(p.F384L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154869445:154869445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520G>A
AA Mutation	p.Ala174Thr(p.A174T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000618040
Start	154772393:154772393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030C>A
AA Mutation	p.Leu344Ile(p.L344I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869896:154869896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.69T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869647:154869647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201079149
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869869:154869869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869314:154869314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764611548
CDS Mutation	c.651G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154725997:154725997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766456980
CDS Mutation	c.1665C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869422:154869422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869260:154869260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.705T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618040
Start	154869315:154869315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.650delC
AA Mutation	p.Pro217ArgfsTer67(p.P217Rfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618040
Start	154869630:154869630(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.335delC
AA Mutation	p.Pro112LeufsTer64(p.P112Lfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000618040
Start	154869697:154869697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268C>T
AA Mutation	p.Gln90Ter(p.Q90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618040
Start	154869314:154869315(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.650dupC
AA Mutation	p.Glu218GlyfsTer21(p.E218Gfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154772258:154772258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165C>T
AA Mutation	p.Arg389Cys(p.R389C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154708139:154708139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371429880
CDS Mutation	c.2078C>T
AA Mutation	p.Ala693Val(p.A693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618040
Start	154708224:154708224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993G>A
AA Mutation	p.Glu665Lys(p.E665K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618040
Start	154869503:154869503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462G>T
Mutation Classification	Silent
Feature Type	Transcript