Colon Cancer: Gene >> SYT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137595:114137595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200072587
CDS Mutation	c.971G>A
AA Mutation	p.Arg324His(p.R324H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137853:114137853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201154501
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137637:114137637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776030947
CDS Mutation	c.929G>A
AA Mutation	p.Arg310His(p.R310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137810:114137810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756G>T
AA Mutation	p.Lys252Asn(p.K252N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114153660:114153660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113G>A
AA Mutation	p.Arg38Gln(p.R38Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610222
Start	114103677:114103677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610222
Start	114103716:114103716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368052418
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SYT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137604:114137604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549305784
CDS Mutation	c.962G>A
AA Mutation	p.Arg321His(p.R321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137854:114137854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Cys(p.R238C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137839:114137839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727A>G
AA Mutation	p.Thr243Ala(p.T243A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114137927:114137927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639G>T
AA Mutation	p.Lys213Asn(p.K213N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610222
Start	114139868:114139868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259C>T
AA Mutation	p.Pro87Ser(p.P87S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610222
Start	114139650:114139650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>T
Mutation Classification	Silent
Feature Type	Transcript