Colon Cancer: Gene >> MCMBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360003
Start	119859166:119859166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360003
Start	119847652:119847652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788C>T
AA Mutation	p.Ser263Phe(p.S263F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360003
Start	119836918:119836918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526C>T
AA Mutation	p.Ser509Leu(p.S509L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360003
Start	119831586:119831586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817G>T
AA Mutation	p.Ser606Ile(p.S606I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360003
Start	119849498:119849498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653C>A
AA Mutation	p.Ser218Tyr(p.S218Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360003
Start	119859121:119859121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139316442
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Cys(p.R69C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360003
Start	119835615:119835615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360003
Start	119835666:119835666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1587A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360003
Start	119853108:119853108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765203487
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000360003
Start	119857340:119857340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>T
AA Mutation	p.Glu143Ter(p.E143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000360003
Start	119840869:119840869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222C>T
AA Mutation	p.Arg408Ter(p.R408*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360003
Start	119858882:119858882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MCMBP

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360003
Start	119836905:119836905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000360003
Start	119837030:119837030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1415-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript