Colon Cancer: Gene >> KCNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673911:110673911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>T
AA Mutation	p.Thr300Met(p.T300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110674427:110674427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>T
AA Mutation	p.Thr128Met(p.T128M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673956:110673956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854G>A
AA Mutation	p.Arg285His(p.R285H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673602:110673602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1208T>C
AA Mutation	p.Phe403Ser(p.F403S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673978:110673978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832G>A
AA Mutation	p.Gly278Ser(p.G278S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673248:110673248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562A>T
AA Mutation	p.Asn521Ile(p.N521I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110674011:110674011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673444:110673444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366G>T
AA Mutation	p.Gly456Trp(p.G456W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673566:110673566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244C>T
AA Mutation	p.Ala415Val(p.A415V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673590:110673590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220T>C
AA Mutation	p.Ile407Thr(p.I407T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673165:110673165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1645A>G
AA Mutation	p.Thr549Ala(p.T549A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673711:110673711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Cys(p.R367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673100:110673100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1710G>T
AA Mutation	p.Lys570Asn(p.K570N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673399:110673399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411A>G
AA Mutation	p.Thr471Ala(p.T471A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110674404:110674404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Cys(p.R136C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673674:110673674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379His(p.R379H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110673214:110673214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110673886:110673886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110674528:110674528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110673568:110673568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110674342:110674342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750178275
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110674417:110674417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756473605
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369769
Start	110673961:110673961(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.849delG
AA Mutation	p.Ser284ProfsTer45(p.S284Pfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000369769
Start	110674369:110674369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>A
AA Mutation	p.Tyr147Ter(p.Y147*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KCNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673213:110673213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597G>A
AA Mutation	p.Glu533Lys(p.E533K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673381:110673381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429C>T
AA Mutation	p.Pro477Ser(p.P477S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673230:110673230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1580C>T
AA Mutation	p.Ser527Leu(p.S527L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369769
Start	110673815:110673815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995A>G
AA Mutation	p.Asp332Gly(p.D332G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110673988:110673988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110674353:110674353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369769
Start	110673967:110673967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.843G>A
Mutation Classification	Silent
Feature Type	Transcript