Colon Cancer: Gene >> MLXIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319080
Start	122130103:122130103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Trp(p.R301W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319080
Start	122137567:122137567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2131C>T
AA Mutation	p.Pro711Ser(p.P711S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319080
Start	122133424:122133424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169C>T
AA Mutation	p.Ser390Phe(p.S390F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319080
Start	122135321:122135321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319080
Start	122135264:122135264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1773A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319080
Start	122135566:122135566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763369656
CDS Mutation	c.1932C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319080
Start	122127301:122127301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319080
Start	122133722:122133722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1467T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319080
Start	122135561:122135562(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1932dupC
AA Mutation	p.Val645ArgfsTer84(p.V645Rfs*84)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MLXIP

No Mutation Annotation!