Colon Cancer: Gene >> MCU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373053
Start	72884332:72884332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928T>C
AA Mutation	p.Ser310Pro(p.S310P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373053
Start	72871440:72871440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760003771
CDS Mutation	c.721G>A
AA Mutation	p.Ala241Thr(p.A241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373053
Start	72860525:72860525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494G>T
AA Mutation	p.Arg165Ile(p.R165I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373053
Start	72884361:72884361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373053
Start	72884356:72884357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.952_953insTATGT
AA Mutation	p.Asn318IlefsTer19(p.N318Ifs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MCU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373053
Start	72871576:72871576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770146478
CDS Mutation	c.857G>A
AA Mutation	p.Arg286His(p.R286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript