Colon Cancer: Gene >> ABO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133261344:133261344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129G>A
AA Mutation	p.Met43Ile(p.M43I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133256247:133256247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481G>A
AA Mutation	p.Val161Met(p.V161M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133255860:133255860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781789696
CDS Mutation	c.868G>A
AA Mutation	p.Asp290Asn(p.D290N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133256142:133256142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586G>A
AA Mutation	p.Glu196Lys(p.E196K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133255842:133255842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370138477
CDS Mutation	c.886G>A
AA Mutation	p.Glu296Lys(p.E296K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133257418:133257418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362C>A
AA Mutation	p.Ala121Asp(p.A121D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133262151:133262151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46G>A
AA Mutation	p.Ala16Thr(p.A16T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133255799:133255799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929T>C
AA Mutation	p.Leu310Pro(p.L310P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000611156
Start	133256172:133256172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Cys(p.R186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611156
Start	133256104:133256104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782686085
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611156
Start	133262110:133262110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ABO

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611156
Start	133255951:133255951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript