Colon Cancer: Gene >> RHOQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238738
Start	46580964:46580964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499A>G
AA Mutation	p.Thr167Ala(p.T167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238738
Start	46576090:46576090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205G>T
AA Mutation	p.Asp69Tyr(p.D69Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238738
Start	46543780:46543780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169T>C
AA Mutation	p.Tyr57His(p.Y57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238738
Start	46576578:46576578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750487279
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238738
Start	46580942:46580942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238738
Start	46543172:46543172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238738
Start	46543758:46543758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372730370
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000238738
Start	46581035:46581035(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.577delA
AA Mutation	p.Arg193GlufsTer2(p.R193Efs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000238738
Start	46580986:46580986(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.525delT
AA Mutation	p.Phe175LeufsTer6(p.F175Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RHOQ

No Mutation Annotation!