Colon Cancer: Gene >> RGS17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153011714:153011714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493G>A
AA Mutation	p.Asp165Asn(p.D165N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153024442:153024442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264G>T
AA Mutation	p.Met88Ile(p.M88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153011641:153011641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566G>T
AA Mutation	p.Arg189Met(p.R189M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153024334:153024334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372G>T
AA Mutation	p.Gln124His(p.Q124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153024474:153024474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>A
AA Mutation	p.Val78Ile(p.V78I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206262
Start	153026477:153026477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000206262
Start	153011575:153011575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206262
Start	153043911:153043911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RGS17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153024379:153024379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327G>T
AA Mutation	p.Glu109Asp(p.E109D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000206262
Start	153011654:153011654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>T
AA Mutation	p.Asp185Tyr(p.D185Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206262
Start	153011676:153011676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript