Colon Cancer: Gene >> MON1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77193675:77193675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Trp(p.R125W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194929:77194929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372814782
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194883:77194883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751690285
CDS Mutation	c.1024C>T
AA Mutation	p.Arg342Cys(p.R342C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194656:77194656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776828713
CDS Mutation	c.797G>A
AA Mutation	p.Arg266Gln(p.R266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194958:77194958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Trp(p.R367W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77198289:77198289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763233279
CDS Mutation	c.1625G>A
AA Mutation	p.Gly542Asp(p.G542D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194379:77194379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750058319
CDS Mutation	c.520G>A
AA Mutation	p.Val174Met(p.V174M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194647:77194647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374115505
CDS Mutation	c.788C>T
AA Mutation	p.Ala263Val(p.A263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77194995:77194995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755287354
CDS Mutation	c.1136C>T
AA Mutation	p.Ala379Val(p.A379V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77198121:77198121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457T>G
AA Mutation	p.Phe486Cys(p.F486C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77198216:77198216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752840417
CDS Mutation	c.1552C>T
AA Mutation	p.Arg518Trp(p.R518W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77198228:77198228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1564C>T
AA Mutation	p.Arg522Cys(p.R522C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77193522:77193522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>T
AA Mutation	p.Arg74Trp(p.R74W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248248
Start	77198122:77198122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MON1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248248
Start	77191507:77191507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22G>A
AA Mutation	p.Ala8Thr(p.A8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript