Colon Cancer: Gene >> MICU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382374
Start	21566884:21566884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271A>G
AA Mutation	p.Met91Val(p.M91V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382374
Start	21603980:21603980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.169A>C
AA Mutation	p.Ser57Arg(p.S57R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382374
Start	21510056:21510056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191372140
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382374
Start	21539372:21539372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382374
Start	21495242:21495242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1119C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000382374
Start	21493251:21493251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1303delT
AA Mutation	p.Ter435Asn(p.*435N)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382374
Start	21502990:21502990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773735238
CDS Mutation	c.869delT
AA Mutation	p.Phe290SerfsTer14(p.F290Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000382374
Start	21495286:21495286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075G>T
AA Mutation	p.Gly359Ter(p.G359*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000382374
Start	21510008:21510008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772353232
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Ter(p.R253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382374
Start	21521258:21521259(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.583dupA
AA Mutation	p.Arg195LysfsTer5(p.R195Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MICU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382374
Start	21539317:21539317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>T
AA Mutation	p.Asp151Tyr(p.D151Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000382374
Start	21510008:21510008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772353232
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Ter(p.R253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript