Colon Cancer: Gene >> SYN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47574744:47574744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446His(p.R446H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47605020:47605020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732C>A
AA Mutation	p.Phe244Leu(p.F244L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47574033:47574033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1951G>A
AA Mutation	p.Ala651Thr(p.A651T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47576535:47576535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762952014
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Cys(p.R315C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47606989:47606989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483C>A
AA Mutation	p.Phe161Leu(p.F161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295987
Start	47576563:47576563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295987
Start	47575215:47575215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295987
Start	47619711:47619711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295987
Start	47574016:47574016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199844514
CDS Mutation	c.1968G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295987
Start	47575152:47575152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295987
Start	47576167:47576167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757867825
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000295987
Start	47619437:47619437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>T
AA Mutation	p.Gln98Ter(p.Q98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SYN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47605051:47605051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701G>A
AA Mutation	p.Arg234Gln(p.R234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47577459:47577459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760401568
CDS Mutation	c.817G>A
AA Mutation	p.Ala273Thr(p.A273T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295987
Start	47605012:47605012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740T>C
AA Mutation	p.Ile247Thr(p.I247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000295987
Start	47605025:47605025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>T
AA Mutation	p.Glu243Ter(p.E243*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript