Colon Cancer: Gene >> MICU3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318063
Start	17116460:17116460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182707903
CDS Mutation	c.1384G>A
AA Mutation	p.Val462Ile(p.V462I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318063
Start	17105561:17105561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143132509
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Cys(p.R412C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318063
Start	17105562:17105562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774411224
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318063
Start	17105416:17105416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089C>A
AA Mutation	p.Phe363Leu(p.F363L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318063
Start	17116518:17116518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442T>G
AA Mutation	p.Ile481Ser(p.I481S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318063
Start	17104423:17104423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318063
Start	17077830:17077830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750645681
CDS Mutation	c.615A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318063
Start	17085310:17085310(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.773delT
AA Mutation	p.Leu258TrpfsTer57(p.L258Wfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000318063
Start	17077843:17077843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150021056
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Ter(p.R210*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MICU3

No Mutation Annotation!