Colon Cancer: Gene >> FUBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77966914:77966914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385G>A
AA Mutation	p.Glu129Lys(p.E129K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77964096:77964096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007C>T
AA Mutation	p.Ala336Val(p.A336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370768
Start	77955257:77955257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1778T>C
AA Mutation	p.Met593Thr(p.M593T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77978991:77978991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Ser5Leu(p.S5L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77949207:77949207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762248194
CDS Mutation	c.1874A>G
AA Mutation	p.Tyr625Cys(p.Y625C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77978962:77978962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43G>A
AA Mutation	p.Ala15Thr(p.A15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77965124:77965124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581C>T
AA Mutation	p.Ala194Val(p.A194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370768
Start	77965156:77965156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758508471
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370768
Start	77967644:77967644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375397592
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370768
Start	77949161:77949161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1920A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370768
Start	77960364:77960364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1476A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370768
Start	77978975:77978975(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.30delC
AA Mutation	p.Ser11LeufsTer43(p.S11Lfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370768
Start	77964293:77964293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.901delA
AA Mutation	p.Ile301TyrfsTer22(p.I301Yfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FUBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370768
Start	77956661:77956661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616C>T
AA Mutation	p.Ala539Val(p.A539V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370768
Start	77967644:77967644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375397592
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000370768
Start	77966704:77966704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>T
AA Mutation	p.Glu155Ter(p.E155*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000370768
Start	77970016:77970016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181446878
CDS Mutation	c.121-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript