Colon Cancer: Gene >> RGS7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240936698:240936698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
AA Mutation	p.Leu79Phe(p.L79F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000366565
Start	240870117:240870117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770058894
CDS Mutation	c.388G>A
AA Mutation	p.Val130Ile(p.V130I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240806246:240806246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163T>G
AA Mutation	p.Phe388Cys(p.F388C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240813685:240813685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889C>A
AA Mutation	p.Leu297Ile(p.L297I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000366565
Start	240816414:240816414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686C>A
AA Mutation	p.Ser229Tyr(p.S229Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240811922:240811922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078T>G
AA Mutation	p.Leu360Val(p.L360V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366565
Start	240811995:240811995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776954930
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366565
Start	240806227:240806227(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1182delC
AA Mutation	p.Ser395ValfsTer17(p.S395Vfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366565
Start	241355737:241355737(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.40delG
AA Mutation	p.Val14TrpfsTer18(p.V14Wfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366565
Start	240814735:240814735(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.826delA
AA Mutation	p.Met276CysfsTer9(p.M276Cfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000366565
Start	240812039:240812039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>T
AA Mutation	p.Glu321Ter(p.E321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RGS7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240802910:240802910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>T
AA Mutation	p.Lys451Asn(p.K451N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240814744:240814744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772169550
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Trp(p.R273W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366565
Start	240827162:240827162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620T>C
AA Mutation	p.Val207Ala(p.V207A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript