Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38363998:38363998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545550026
CDS Mutation	c.676G>A
AA Mutation	p.Ala226Thr(p.A226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38369109:38369109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>A
AA Mutation	p.Ala366Thr(p.A366T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38349640:38349640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374882159
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Cys(p.R73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38346541:38346541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25C>T
AA Mutation	p.Pro9Ser(p.P9S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38369053:38369053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374549700
CDS Mutation	c.1040C>T
AA Mutation	p.Pro347Leu(p.P347L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38364744:38364744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>A
AA Mutation	p.Asp305Asn(p.D305N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217407
Start	38364623:38364623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38346610:38346610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140031031
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217407
Start	38354405:38354405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139250125
CDS Mutation	c.490G>A
AA Mutation	p.Ala164Thr(p.A164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217407
Start	38354428:38354428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760833819
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217407
Start	38346543:38346543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148521627
CDS Mutation	c.27G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217407
Start	38354404:38354404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript