Colon Cancer: Gene >> AASDHPPT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278618
Start	106096855:106096855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878A>T
AA Mutation	p.Asp293Val(p.D293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278618
Start	106090559:106090559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Cys(p.R138C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278618
Start	106077796:106077796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>A
AA Mutation	p.Ser29Asn(p.S29N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278618
Start	106096775:106096775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000278618
Start	106091370:106091370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586C>T
AA Mutation	p.Gln196Ter(p.Q196*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AASDHPPT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278618
Start	106077871:106077871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278618
Start	106079582:106079582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299A>C
AA Mutation	p.Asn100Thr(p.N100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278618
Start	106091410:106091410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626T>C
AA Mutation	p.Ile209Thr(p.I209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278618
Start	106079592:106079592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775262240
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript