Colon Cancer: Gene >> ZRANB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124966720:124966720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Ile(p.T314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124943037:124943037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124942876:124942876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>C
AA Mutation	p.Arg128Thr(p.R128T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124984852:124984852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987G>A
AA Mutation	p.Ala663Thr(p.A663T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124942549:124942549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56C>A
AA Mutation	p.Pro19Gln(p.P19Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124942764:124942764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.His91Tyr(p.H91Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124942576:124942576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567970870
CDS Mutation	c.83G>A
AA Mutation	p.Arg28His(p.R28H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124942555:124942555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62C>T
AA Mutation	p.Ala21Val(p.A21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000359653
Start	124943043:124943043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>T
AA Mutation	p.Glu184Ter(p.E184*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359653
Start	124983576:124983577(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1798dupC
AA Mutation	p.Arg600ProfsTer6(p.R600Pfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359653
Start	124984850:124984851(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1985_1986insAGGAATG
AA Mutation	p.Ala663GlyfsTer25(p.A663Gfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000359653
Start	124983653:124983654(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1875_1876insAAAGAG
AA Mutation	p.Lys625_Leu626insLysGlu(p.K625_L626insKE)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZRANB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124983470:124983470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1690C>T
AA Mutation	p.Pro564Ser(p.P564S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359653
Start	124971976:124971976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1014A>T
AA Mutation	p.Gln338His(p.Q338H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript