Colon Cancer: Gene >> KCNA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044529:5044529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382G>A
AA Mutation	p.Gly128Arg(p.G128R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044736:5044736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>A
AA Mutation	p.Ala197Thr(p.A197T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045126:5045126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>A
AA Mutation	p.Val327Met(p.V327M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044643:5044643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Asp166Asn(p.D166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044488:5044488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341C>T
AA Mutation	p.Thr114Met(p.T114M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045217:5045217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780720700
CDS Mutation	c.1070T>C
AA Mutation	p.Met357Thr(p.M357T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044848:5044848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701G>A
AA Mutation	p.Arg234His(p.R234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044892:5044892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>A
AA Mutation	p.Ala249Thr(p.A249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045171:5045171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1024C>T
AA Mutation	p.Arg342Cys(p.R342C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044668:5044668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>A
AA Mutation	p.Gly174Asp(p.G174D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045013:5045013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866A>G
AA Mutation	p.His289Arg(p.H289R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044782:5044782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>A
AA Mutation	p.Arg212His(p.R212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045354:5045354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Cys(p.R403C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045270:5045270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123G>A
AA Mutation	p.Glu375Lys(p.E375K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045141:5045141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994G>A
AA Mutation	p.Val332Ile(p.V332I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044760:5044760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613C>G
AA Mutation	p.Leu205Val(p.L205V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044263:5044263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116C>T
AA Mutation	p.Thr39Met(p.T39M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044454:5044454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>A
AA Mutation	p.Gly103Ser(p.G103S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044664:5044664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517G>A
AA Mutation	p.Asp173Asn(p.D173N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045555:5045555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408G>A
AA Mutation	p.Ala470Thr(p.A470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044847:5044847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747919632
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Cys(p.R234C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045640:5045640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145163163
CDS Mutation	c.1493C>T
AA Mutation	p.Ser498Leu(p.S498L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5044546:5044546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752249172
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5045137:5045137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5044666:5044666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752478454
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5044729:5044729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5045044:5045044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773608258
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5044780:5044780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252321
Start	5045846:5045846(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1704delG
AA Mutation	p.Thr569ProfsTer15(p.T569Pfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KCNA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045207:5045207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746268474
CDS Mutation	c.1060C>T
AA Mutation	p.Arg354Trp(p.R354W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044647:5044647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770186331
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5044736:5044736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>A
AA Mutation	p.Ala197Thr(p.A197T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252321
Start	5045373:5045373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409His(p.R409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5045692:5045692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5044864:5044864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252321
Start	5045641:5045641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576837393
CDS Mutation	c.1494G>A
Mutation Classification	Silent
Feature Type	Transcript