Colon Cancer: Gene >> UIMC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377227
Start	176970749:176970749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350G>T
AA Mutation	p.Ser117Ile(p.S117I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377227
Start	176907114:176907114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912G>A
AA Mutation	p.Asp638Asn(p.D638N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377227
Start	176969008:176969008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377227
Start	176968630:176968630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377227
Start	176975448:176975448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377227
Start	176905330:176905330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000377227
Start	176905407:176905408(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2034_2035insTACTAATGGTTTT
AA Mutation	p.Val679TyrfsTer2(p.V679Yfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UIMC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377227
Start	176969699:176969699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779796802
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377227
Start	176968701:176968701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>T
AA Mutation	p.Asp352Tyr(p.D352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript