Colon Cancer: Gene >> ZBTB49

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4321015:4321015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997A>G
AA Mutation	p.Asp666Gly(p.D666G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4321048:4321048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2030T>G
AA Mutation	p.Leu677Arg(p.L677R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4320807:4320807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789G>A
AA Mutation	p.Glu597Lys(p.E597K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4315864:4315864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515A>C
AA Mutation	p.Lys505Asn(p.K505N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4302797:4302797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750086879
CDS Mutation	c.961G>T
AA Mutation	p.Ala321Ser(p.A321S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4302513:4302513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677A>G
AA Mutation	p.Lys226Arg(p.K226R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4313086:4313086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348C>A
AA Mutation	p.Pro450Thr(p.P450T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337872
Start	4302463:4302463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337872
Start	4303021:4303021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375472556
CDS Mutation	c.1185C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337872
Start	4302217:4302217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337872
Start	4320842:4320842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749749313
CDS Mutation	c.1824C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000337872
Start	4315715:4315715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456C>T
AA Mutation	p.Arg486Ter(p.R486*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337872
Start	4315893:4315894(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1548dupT
AA Mutation	p.Asn517Ter(p.N517*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB49

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4302060:4302060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145711052
CDS Mutation	c.224T>C
AA Mutation	p.Ile75Thr(p.I75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337872
Start	4302931:4302931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095G>T
AA Mutation	p.Glu365Asp(p.E365D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337872
Start	4302664:4302664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript