Colon Cancer: Gene >> KIF4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70290760:70290760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190G>A
AA Mutation	p.Val64Ile(p.V64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70343713:70343713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773017445
CDS Mutation	c.1277C>T
AA Mutation	p.Ala426Val(p.A426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70353679:70353679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546G>T
AA Mutation	p.Ala516Ser(p.A516S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70301909:70301909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526C>T
AA Mutation	p.Leu176Phe(p.L176F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70403978:70403978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768717763
CDS Mutation	c.2734A>C
AA Mutation	p.Ile912Leu(p.I912L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70290496:70290496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38C>T
AA Mutation	p.Ala13Val(p.A13V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70302369:70302369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749C>T
AA Mutation	p.Thr250Ile(p.T250I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70402598:70402598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2522T>C
AA Mutation	p.Leu841Pro(p.L841P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70376131:70376131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35473790
CDS Mutation	c.1955G>A
AA Mutation	p.Arg652His(p.R652H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70406905:70406905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3085C>T
AA Mutation	p.Arg1029Cys(p.R1029C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70302387:70302387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767G>A
AA Mutation	p.Arg256His(p.R256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70329501:70329501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875A>C
AA Mutation	p.Lys292Thr(p.K292T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70353746:70353746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613C>T
AA Mutation	p.Ala538Val(p.A538V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70404031:70404031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2787G>T
AA Mutation	p.Glu929Asp(p.E929D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70406990:70406990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3170A>G
AA Mutation	p.Asp1057Gly(p.D1057G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70297125:70297125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70374189:70374189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1713G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70375315:70375315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1890G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70403926:70403926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2682C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70420079:70420079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70329418:70329418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70405881:70405881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2952C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374403
Start	70420233:70420233(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3668delG
AA Mutation	p.Gly1223AlafsTer37(p.G1223Afs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000374403
Start	70396030:70396030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2470G>T
AA Mutation	p.Glu824Ter(p.E824*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374403
Start	70376174:70376175(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2004dupA
AA Mutation	p.Asp669ArgfsTer13(p.D669Rfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70290561:70290561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>A
AA Mutation	p.Val35Met(p.V35M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70301990:70301990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607A>G
AA Mutation	p.Thr203Ala(p.T203A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70299127:70299127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441A>C
AA Mutation	p.Glu147Asp(p.E147D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70330277:70330277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016A>C
AA Mutation	p.Lys339Thr(p.K339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70420079:70420079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3513C>T
Mutation Classification	Silent
Feature Type	Transcript