Colon Cancer: Gene >> ZBTB38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141445425:141445425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200031071
CDS Mutation	c.3037G>A
AA Mutation	p.Glu1013Lys(p.E1013K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141444415:141444415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2027C>A
AA Mutation	p.Ser676Tyr(p.S676Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141445048:141445048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2660G>A
AA Mutation	p.Ser887Asn(p.S887N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141443400:141443400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012C>T
AA Mutation	p.Pro338Ser(p.P338S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141442467:141442467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79C>T
AA Mutation	p.Arg27Cys(p.R27C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141444994:141444994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2606A>G
AA Mutation	p.Gln869Arg(p.Q869R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141445357:141445357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2969A>G
AA Mutation	p.Asp990Gly(p.D990G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141444318:141444318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1930T>G
AA Mutation	p.Ser644Ala(p.S644A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141443607:141443607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201269241
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Cys(p.R407C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141445411:141445411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3023G>A
AA Mutation	p.Arg1008Gln(p.R1008Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141444153:141444153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765G>A
AA Mutation	p.Ala589Thr(p.A589T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321464
Start	141443168:141443168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748455361
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321464
Start	141442424:141442424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773460161
CDS Mutation	c.36C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321464
Start	141445692:141445692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3304A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321464
Start	141445268:141445268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772563785
CDS Mutation	c.2880C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321464
Start	141444890:141444890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2502A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321464
Start	141442837:141442837(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.454delA
AA Mutation	p.Arg152GlyfsTer34(p.R152Gfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321464
Start	141442926:141442926(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.541delT
AA Mutation	p.Ser181ProfsTer5(p.S181Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321464
Start	141442399:141442400(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.12dupG
AA Mutation	p.Ser5ValfsTer13(p.S5Vfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321464
Start	141443725:141443725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337A>C
AA Mutation	p.Asp446Ala(p.D446A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321464
Start	141444791:141444791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2403A>C
Mutation Classification	Silent
Feature Type	Transcript