Colon Cancer: Gene >> LTBR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6384447:6384447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89C>T
AA Mutation	p.Pro30Leu(p.P30L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6386152:6386152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559C>G
AA Mutation	p.Pro187Ala(p.P187A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6386396:6386396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Asp207Asn(p.D207N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6386147:6386147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554G>A
AA Mutation	p.Cys185Tyr(p.C185Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6390853:6390853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224G>T
AA Mutation	p.Lys408Asn(p.K408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6386131:6386131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538T>C
AA Mutation	p.Ser180Pro(p.S180P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6390238:6390238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759292715
CDS Mutation	c.928G>A
AA Mutation	p.Ala310Thr(p.A310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228918
Start	6384641:6384641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228918
Start	6386386:6386386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228918
Start	6388417:6388417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228918
Start	6386132:6386132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.543delC
AA Mutation	p.Ser182AlafsTer33(p.S182Afs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000228918
Start	6385103:6385103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275G>A
AA Mutation	p.Trp92Ter(p.W92*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LTBR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228918
Start	6385305:6385305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Ala133Val(p.A133V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript