Colon Cancer: Gene >> UBTF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44211322:44211322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057G>T
AA Mutation	p.Asp353Tyr(p.D353Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44211650:44211650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>A
AA Mutation	p.Leu335Met(p.L335M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44210422:44210422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766049083
CDS Mutation	c.1411C>T
AA Mutation	p.Pro471Ser(p.P471S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44210388:44210388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445C>T
AA Mutation	p.Pro482Leu(p.P482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44210397:44210397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436G>A
AA Mutation	p.Gly479Asp(p.G479D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44210425:44210425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408A>G
AA Mutation	p.Lys470Glu(p.K470E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44209381:44209381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876T>C
AA Mutation	p.Tyr626His(p.Y626H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44211300:44211300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44216686:44216686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77A>G
AA Mutation	p.Asp26Gly(p.D26G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302904
Start	44207263:44207263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2274C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302904
Start	44211726:44211726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139786333
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302904
Start	44207556:44207556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2067C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302904
Start	44207592:44207592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763153058
CDS Mutation	c.2031C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302904
Start	44216573:44216574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.189_190delTT
AA Mutation	p.Ser64TrpfsTer13(p.S64Wfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UBTF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302904
Start	44211326:44211326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053G>T
AA Mutation	p.Lys351Asn(p.K351N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302904
Start	44215735:44215735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript