Colon Cancer: Gene >> SLC30A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396591
Start	69123267:69123267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747904806
CDS Mutation	c.1840G>C
AA Mutation	p.Glu614Gln(p.E614Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396591
Start	69116169:69116169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145568710
CDS Mutation	c.1027G>A
AA Mutation	p.Val343Ile(p.V343I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69121747:69121747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69118559:69118559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199655047
CDS Mutation	c.1500G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69108367:69108367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69123287:69123287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200016525
CDS Mutation	c.1860C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69100867:69100867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201023507
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000396591
Start	69128027:69128029(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2024_2026delCAT
AA Mutation	p.Ser675del(p.S675del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC30A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396591
Start	69118558:69118558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768665809
CDS Mutation	c.1499C>T
AA Mutation	p.Ala500Val(p.A500V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69100867:69100867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201023507
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396591
Start	69116515:69116515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript