Colon Cancer: Gene >> RGS11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397770
Start	275029:275029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Cys(p.R89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397770
Start	271023:271023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747085732
CDS Mutation	c.940C>T
AA Mutation	p.Arg314Trp(p.R314W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397770
Start	270545:270545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184A>G
AA Mutation	p.His395Arg(p.H395R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397770
Start	271061:271061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902G>A
AA Mutation	p.Gly301Asp(p.G301D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397770
Start	273532:273532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397770
Start	275048:275048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397770
Start	273530:273531(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764258115
CDS Mutation	c.532dupG
AA Mutation	p.Asp178GlyfsTer50(p.D178Gfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RGS11

No Mutation Annotation!