Colon Cancer: Gene >> TP63

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189808326:189808326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375508394
CDS Mutation	c.379G>A
AA Mutation	p.Gly127Ser(p.G127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189894452:189894452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1993A>G
AA Mutation	p.Met665Val(p.M665V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189808444:189808444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497C>T
AA Mutation	p.Pro166Leu(p.P166L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189808468:189808468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201188464
CDS Mutation	c.521C>T
AA Mutation	p.Pro174Leu(p.P174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189738752:189738752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755677647
CDS Mutation	c.302C>T
AA Mutation	p.Ser101Leu(p.S101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264731
Start	189868716:189868716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576449010
CDS Mutation	c.1129C>T
AA Mutation	p.Pro377Ser(p.P377S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189886529:189886529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1485T>G
AA Mutation	p.Ile495Met(p.I495M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189868615:189868615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121908841
CDS Mutation	c.1028G>A
AA Mutation	p.Arg343Gln(p.R343Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189872899:189872899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253A>G
AA Mutation	p.Lys418Arg(p.K418R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808469:189808469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780233345
CDS Mutation	c.522G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808394:189808394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772653802
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189894409:189894409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1950C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808436:189808436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808400:189808400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808283:189808283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267599728
CDS Mutation	c.336G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808346:189808346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145730343
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189808478:189808478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000264731
Start	189894239:189894239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Ter(p.R594*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000264731
Start	189866711:189866711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Ter(p.R266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264731
Start	189868717:189868717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376910274
CDS Mutation	c.1129+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TP63

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189808381:189808381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>T
AA Mutation	p.Ala145Val(p.A145V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189864411:189864411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759C>A
AA Mutation	p.Phe253Leu(p.F253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264731
Start	189890792:189890792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656C>A
AA Mutation	p.Phe552Leu(p.F552L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264731
Start	189889434:189889434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780464690
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000264731
Start	189737819:189737819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142G>T
AA Mutation	p.Glu48Ter(p.E48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000264731
Start	189866744:189866744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829G>T
AA Mutation	p.Glu277Ter(p.E277*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript