Colon Cancer: Gene >> RGS10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369101
Start	119500163:119500163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752336933
CDS Mutation	c.472C>T
AA Mutation	p.Pro158Ser(p.P158S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369101
Start	119500148:119500148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487G>A
AA Mutation	p.Ala163Thr(p.A163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369101
Start	119515601:119515601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283T>G
AA Mutation	p.Ser95Ala(p.S95A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369101
Start	119500227:119500227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369101
Start	119515614:119515614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000369101
Start	119526091:119526091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>T
AA Mutation	p.Glu58Ter(p.E58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369101
Start	119526055:119526056(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.207dupT
AA Mutation	p.Lys70Ter(p.K70*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369101
Start	119526048:119526049(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.214dupA
AA Mutation	p.Met72AsnfsTer4(p.M72Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RGS10

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000369101
Start	119526091:119526091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>T
AA Mutation	p.Glu58Ter(p.E58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript