Colon Cancer: Gene >> MLC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50061600:50061600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>C
AA Mutation	p.Val373Leu(p.V373L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50061611:50061611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106G>A
AA Mutation	p.Arg369Lys(p.R369K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50076894:50076894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537457768
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50084827:50084827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201522059
CDS Mutation	c.76G>A
AA Mutation	p.Ala26Thr(p.A26T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50068465:50068465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862G>C
AA Mutation	p.Glu288Gln(p.E288Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50076879:50076879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761502278
CDS Mutation	c.559G>A
AA Mutation	p.Glu187Lys(p.E187K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50074295:50074295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>C
AA Mutation	p.Gly212Ala(p.G212A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50084809:50084809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193115579
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50061606:50061606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200273593
CDS Mutation	c.1111G>A
AA Mutation	p.Val371Ile(p.V371I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311597
Start	50076895:50076895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559021124
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311597
Start	50064055:50064055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756949575
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311597
Start	50084768:50084768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.135delC
AA Mutation	p.Cys46AlafsTer12(p.C46Afs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MLC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311597
Start	50064134:50064134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs281875313
CDS Mutation	c.959C>T
AA Mutation	p.Thr320Met(p.T320M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311597
Start	50084783:50084783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557978926
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript