Colon Cancer: Gene >> SSTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73169789:73169789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201497830
CDS Mutation	c.470G>A
AA Mutation	p.Arg157Gln(p.R157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73170148:73170148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Val277Ile(p.V277I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73169471:73169471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152T>C
AA Mutation	p.Phe51Ser(p.F51S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73170163:73170163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844A>G
AA Mutation	p.Met282Val(p.M282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73169605:73169605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286C>A
AA Mutation	p.Leu96Met(p.L96M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357585
Start	73169646:73169646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000357585
Start	73169469:73169469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150T>G
AA Mutation	p.Tyr50Ter(p.Y50*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000357585
Start	73170290:73170291(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.998_999insGACATTCTGGAAGCTCTTCTTGAATGTCCTCTGCTTGGTCAAGGTGAG
AA Mutation	p.Val332_Ser333insArgThrPheTrpLysLeuPheLeuAsnValLeuCysLeuValLysVal(p.V332_S333insRTFWKLFLNVLCLVKV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SSTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73169792:73169792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752640995
CDS Mutation	c.473C>T
AA Mutation	p.Thr158Met(p.T158M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357585
Start	73170157:73170157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779626588
CDS Mutation	c.838G>A
AA Mutation	p.Val280Ile(p.V280I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357585
Start	73169466:73169466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147C>A
Mutation Classification	Silent
Feature Type	Transcript