Colon Cancer: Gene >> TP73

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3729411:3729411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>T
AA Mutation	p.Asp387Tyr(p.D387Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3732940:3732940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769809364
CDS Mutation	c.1772G>A
AA Mutation	p.Arg591His(p.R591H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3730119:3730119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760067757
CDS Mutation	c.1316C>T
AA Mutation	p.Ser439Leu(p.S439L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3707639:3707639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757455947
CDS Mutation	c.277G>A
AA Mutation	p.Val93Met(p.V93M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3732756:3732756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754162945
CDS Mutation	c.1588G>A
AA Mutation	p.Ala530Thr(p.A530T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3727671:3727671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886G>A
AA Mutation	p.Ala296Thr(p.A296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3732852:3732852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530648280
CDS Mutation	c.1684C>T
AA Mutation	p.Arg562Cys(p.R562C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3730970:3730970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150268231
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3730018:3730018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201857112
CDS Mutation	c.1215G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3707680:3707680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3729398:3729398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776097108
CDS Mutation	c.1146G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3707692:3707692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761898929
CDS Mutation	c.330G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3730994:3730994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750168991
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378295
Start	3731034:3731034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1458delC
AA Mutation	p.Tyr487ThrfsTer11(p.Y487Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378295
Start	3728142:3728142(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1004delC
AA Mutation	p.Pro335LeufsTer10(p.P335Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378295
Start	3730058:3730058(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1259delG
AA Mutation	p.Gly420AlafsTer2(p.G420Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000378295
Start	3729330:3729330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078C>T
AA Mutation	p.Arg360Ter(p.R360*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000378295
Start	3727632:3727632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847C>T
AA Mutation	p.Gln283Ter(p.Q283*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000378295
Start	3729449:3729449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TP73

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3733010:3733010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378295
Start	3683158:3683158(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.164delA
AA Mutation	p.Glu55GlyfsTer3(p.E55Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript