Colon Cancer: Gene >> SIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290399
Start	36699916:36699916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170C>T
AA Mutation	p.Pro57Leu(p.P57L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290399
Start	36726245:36726245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>A
AA Mutation	p.Glu224Lys(p.E224K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290399
Start	36726210:36726210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635C>T
AA Mutation	p.Ala212Val(p.A212V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290399
Start	36744802:36744802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290399
Start	36743462:36743462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111561480
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290399
Start	36709193:36709193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769910823
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290399
Start	36745045:36745045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1489delC
AA Mutation	p.Leu497Ter(p.L497*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290399
Start	36744894:36744894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1334G>A
AA Mutation	p.Gly445Glu(p.G445E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290399
Start	36726217:36726217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771760489
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript