Colon Cancer: Gene >> NGFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49506443:49506443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759353737
CDS Mutation	c.353C>T
AA Mutation	p.Thr118Met(p.T118M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49512923:49512923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534528579
CDS Mutation	c.1198G>A
AA Mutation	p.Ala400Thr(p.A400T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49511995:49511995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>A
AA Mutation	p.Val309Met(p.V309M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49512848:49512848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1123T>C
AA Mutation	p.Ser375Pro(p.S375P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49512044:49512044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116828180
CDS Mutation	c.974C>T
AA Mutation	p.Ser325Leu(p.S325L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49506467:49506467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764232409
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000172229
Start	49510458:49510458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377669981
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000172229
Start	49506543:49506543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000172229
Start	49506549:49506549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000172229
Start	49506564:49506564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000172229
Start	49512976:49512976(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1251delG
AA Mutation	p.Cys418AlafsTer48(p.C418Afs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NGFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000172229
Start	49512845:49512845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120G>T
AA Mutation	p.Asp374Tyr(p.D374Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000172229
Start	49511965:49511965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895G>T
AA Mutation	p.Glu299Ter(p.E299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000172229
Start	49510469:49510470(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.626_627insTG
AA Mutation	p.Pro210AlafsTer16(p.P210Afs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript