Colon Cancer: Gene >> SLC35E1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000595753
Start	16553824:16553824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1088G>A
AA Mutation	p.Ser363Asn(p.S363N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000595753
Start	16566642:16566642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765255227
CDS Mutation	c.646C>T
AA Mutation	p.Arg216Trp(p.R216W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000595753
Start	16572213:16572213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.152T>A
AA Mutation	p.Ile51Asn(p.I51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000595753
Start	16553833:16553833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200335570
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000595753
Start	16568115:16568115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>A
AA Mutation	p.Glu183Lys(p.E183K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595753
Start	16568056:16568056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542109613
CDS Mutation	c.606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595753
Start	16555196:16555196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595753
Start	16555278:16555278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749577127
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595753
Start	16553901:16553901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773244448
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC35E1

No Mutation Annotation!