Colon Cancer: Gene >> SRMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63540865:63540865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420G>A
AA Mutation	p.Ala474Thr(p.A474T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63547399:63547399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777121276
CDS Mutation	c.65C>T
AA Mutation	p.Ala22Val(p.A22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63547271:63547271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764471349
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Trp(p.R65W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63540945:63540945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447His(p.R447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63542554:63542554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142975228
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Trp(p.R225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63542310:63542310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>T
AA Mutation	p.Leu267Phe(p.L267F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63543438:63543438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521C>T
AA Mutation	p.Ala174Val(p.A174V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63542194:63542194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915G>A
AA Mutation	p.Met305Ile(p.M305I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63540826:63540826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146373271
CDS Mutation	c.1459C>T
AA Mutation	p.His487Tyr(p.H487Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63543344:63543344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615G>T
AA Mutation	p.Gln205His(p.Q205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63542460:63542460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137951199
CDS Mutation	c.767C>T
AA Mutation	p.Ala256Val(p.A256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63547402:63547402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564747393
CDS Mutation	c.62C>T
AA Mutation	p.Pro21Leu(p.P21L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217188
Start	63542308:63542308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761533969
CDS Mutation	c.801C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SRMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63547318:63547318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>T
AA Mutation	p.Cys49Phe(p.C49F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63542204:63542204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760106125
CDS Mutation	c.905C>T
AA Mutation	p.Thr302Met(p.T302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217188
Start	63542165:63542165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>T
AA Mutation	p.Gly315Val(p.G315V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217188
Start	63547408:63547408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56T>A
AA Mutation	p.Ile19Asn(p.I19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript