Colon Cancer: Gene >> KCNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911583:4911583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Cys(p.R69C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912081:4912081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>A
AA Mutation	p.Glu235Lys(p.E235K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911598:4911598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>A
AA Mutation	p.Asp74Asn(p.D74N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911886:4911886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912262:4912262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>A
AA Mutation	p.Arg295His(p.R295H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911941:4911941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>T
AA Mutation	p.Thr188Met(p.T188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911539:4911539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Thr54Ile(p.T54I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912055:4912055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28933383
CDS Mutation	c.677C>T
AA Mutation	p.Thr226Met(p.T226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911673:4911673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295G>A
AA Mutation	p.Gly99Ser(p.G99S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912093:4912093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Cys(p.R239C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912094:4912094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748830362
CDS Mutation	c.716G>A
AA Mutation	p.Arg239His(p.R239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911409:4911409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Glu11Lys(p.E11K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911892:4911892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779656199
CDS Mutation	c.514G>A
AA Mutation	p.Val172Ile(p.V172I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912456:4912456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078C>T
AA Mutation	p.Pro360Ser(p.P360S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911685:4911685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Trp(p.R103W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4912424:4912424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046C>T
AA Mutation	p.Ala349Val(p.A349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911544:4911544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911528:4911528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911648:4911648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911522:4911522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4912119:4912119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.741G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911645:4911645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371963908
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911597:4911597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911810:4911810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4912005:4912005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382545
Start	4912274:4912274(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.900delT
AA Mutation	p.Phe300LeufsTer24(p.F300Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382545
Start	4912129:4912129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.755delA
AA Mutation	p.Asn252ThrfsTer3(p.N252Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000382545
Start	4911840:4911840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462G>A
AA Mutation	p.Trp154Ter(p.W154*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KCNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382545
Start	4911487:4911487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>A
AA Mutation	p.Glu37Lys(p.E37K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382545
Start	4911921:4911921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript