Colon Cancer: Gene >> MICU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361114
Start	72533759:72533759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752729268
CDS Mutation	c.524G>A
AA Mutation	p.Arg175His(p.R175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361114
Start	72551221:72551221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>T
AA Mutation	p.Asp151Tyr(p.D151Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361114
Start	72475150:72475150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883A>C
AA Mutation	p.Asn295His(p.N295H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361114
Start	72566735:72566735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59A>G
AA Mutation	p.Tyr20Cys(p.Y20C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361114
Start	72475257:72475257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750157034
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361114
Start	72551300:72551300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361114
Start	72423363:72423363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MICU1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361114
Start	72375870:72375870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183A>G
AA Mutation	p.Thr395Ala(p.T395A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361114
Start	72551221:72551221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>T
AA Mutation	p.Asp151Tyr(p.D151Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript