Colon Cancer: Gene >> SSTR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37207799:37207799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5A>G
AA Mutation	p.Asp2Gly(p.D2G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37207433:37207433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371G>A
AA Mutation	p.Gly124Asp(p.G124D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37207050:37207050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>A
AA Mutation	p.Glu252Lys(p.E252K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37206830:37206830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.974G>T
AA Mutation	p.Arg325Leu(p.R325L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37207586:37207586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748658683
CDS Mutation	c.218C>T
AA Mutation	p.Thr73Met(p.T73M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37206680:37206680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124G>A
AA Mutation	p.Ser375Asn(p.S375N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610913
Start	37207521:37207521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610913
Start	37207210:37207210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776297016
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610913
Start	37206964:37206964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770081383
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610913
Start	37206814:37206814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610913
Start	37206640:37206640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763337226
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SSTR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610913
Start	37206831:37206831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780770327
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Cys(p.R325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript