Colon Cancer: Gene >> SSTR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036468:23036468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760189136
CDS Mutation	c.985C>T
AA Mutation	p.Arg329Cys(p.R329C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035722:23035722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Thr80Met(p.T80M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036619:23036619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372339309
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379His(p.R379H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035943:23035943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036336:23036336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368872232
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035647:23035647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374915518
CDS Mutation	c.164C>T
AA Mutation	p.Ala55Val(p.A55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036186:23036186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>A
AA Mutation	p.Val235Met(p.V235M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035751:23035751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268G>A
AA Mutation	p.Ala90Thr(p.A90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035991:23035991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752836318
CDS Mutation	c.508G>A
AA Mutation	p.Val170Met(p.V170M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036411:23036411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Leu310Phe(p.L310F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036621:23036621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138A>G
AA Mutation	p.Ile380Val(p.I380V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035883:23035883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750847560
CDS Mutation	c.400G>A
AA Mutation	p.Val134Ile(p.V134I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23036215:23036215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369953610
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23036156:23036156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23035678:23035678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23035924:23035924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23035693:23035693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23035966:23035966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SSTR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23035722:23035722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Thr80Met(p.T80M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255008
Start	23036193:23036193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710A>T
AA Mutation	p.Lys237Met(p.K237M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255008
Start	23035708:23035708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764351229
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript