Colon Cancer: Gene >> CNDP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74508899:74508899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149206732
CDS Mutation	c.427G>A
AA Mutation	p.Ala143Thr(p.A143T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74505859:74505859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.215G>A
AA Mutation	p.Gly72Asp(p.G72D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74505906:74505906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771837186
CDS Mutation	c.262G>A
AA Mutation	p.Asp88Asn(p.D88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74500023:74500023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50G>A
AA Mutation	p.Arg17His(p.R17H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74520056:74520056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1416G>T
AA Mutation	p.Gln472His(p.Q472H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74516252:74516252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761637739
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Trp(p.R310W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74518958:74518958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220T>C
AA Mutation	p.Val407Ala(p.V407A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74510843:74510843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Glu163Lys(p.E163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74513616:74513616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800C>T
AA Mutation	p.Ala267Val(p.A267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324262
Start	74518995:74518995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772283834
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CNDP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324262
Start	74511007:74511007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651C>A
AA Mutation	p.Phe217Leu(p.F217L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324262
Start	74518567:74518567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript