Colon Cancer: Gene >> TFAP2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56637858:56637858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198T>A
AA Mutation	p.Phe400Ile(p.F400I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56634235:56634235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150059207
CDS Mutation	c.889G>A
AA Mutation	p.Ala297Thr(p.A297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56637814:56637814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760198839
CDS Mutation	c.1154A>G
AA Mutation	p.Asn385Ser(p.N385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56636706:56636706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019G>A
AA Mutation	p.Gly340Glu(p.G340E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56631235:56631235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79C>A
AA Mutation	p.Pro27Thr(p.P27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56633520:56633520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754T>C
AA Mutation	p.Ser252Pro(p.S252P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56631358:56631358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Ala68Thr(p.A68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56631409:56631409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56631371:56631371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215C>T
AA Mutation	p.Ser72Leu(p.S72L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000201031
Start	56631687:56631687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TFAP2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56631820:56631820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748899621
CDS Mutation	c.550C>T
AA Mutation	p.His184Tyr(p.H184Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56634215:56634215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869C>T
AA Mutation	p.Pro290Leu(p.P290L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000201031
Start	56637989:56637989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>T
AA Mutation	p.Glu443Asp(p.E443D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript