Colon Cancer: Gene >> SSTR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38210324:38210324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.935G>T
AA Mutation	p.Gly312Val(p.G312V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209895:38209895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506G>A
AA Mutation	p.Arg169His(p.R169H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38210428:38210428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1039G>T
AA Mutation	p.Ala347Ser(p.A347S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209663:38209663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757226690
CDS Mutation	c.274G>A
AA Mutation	p.Ala92Thr(p.A92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209648:38209648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>A
AA Mutation	p.Ala87Thr(p.A87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209690:38209690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301G>A
AA Mutation	p.Ala101Thr(p.A101T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38210000:38210000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>C
AA Mutation	p.Gly204Ala(p.G204A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209798:38209798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546561451
CDS Mutation	c.409G>A
AA Mutation	p.Asp137Asn(p.D137N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38210471:38210471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082G>A
AA Mutation	p.Arg361His(p.R361H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209906:38209906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Val173Met(p.V173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38210427:38210427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38210055:38210055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38209800:38209800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38210424:38210424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767718814
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38209929:38209929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38210337:38210337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SSTR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267377
Start	38209921:38209921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532A>C
AA Mutation	p.Asn178His(p.N178H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267377
Start	38209662:38209662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript