Colon Cancer: Gene >> MANBA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102722993:102722993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145950049
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Cys(p.R143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102664699:102664699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1471G>C
AA Mutation	p.Glu491Gln(p.E491Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102714494:102714494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.617G>T
AA Mutation	p.Arg206Ile(p.R206I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102690603:102690603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842T>C
AA Mutation	p.Ile281Thr(p.I281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102723907:102723907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333C>A
AA Mutation	p.Phe111Leu(p.F111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102690706:102690706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>A
AA Mutation	p.Val247Ile(p.V247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102634882:102634882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2321A>G
AA Mutation	p.Tyr774Cys(p.Y774C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226578
Start	102690689:102690689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779421094
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226578
Start	102632174:102632174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2523C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226578
Start	102722919:102722919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226578
Start	102634824:102634824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372595764
CDS Mutation	c.2379G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226578
Start	102639837:102639837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000226578
Start	102689685:102689685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MANBA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226578
Start	102664693:102664693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561172083
CDS Mutation	c.1477G>A
AA Mutation	p.Val493Ile(p.V493I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226578
Start	102722892:102722892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000226578
Start	102673946:102673946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085C>A
AA Mutation	p.Ser362Ter(p.S362*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript