Colon Cancer: Gene >> SLC5A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266088
Start	32110149:32110149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1931T>C
AA Mutation	p.Val644Ala(p.V644A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266088
Start	32102068:32102068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1496G>A
AA Mutation	p.Arg499His(p.R499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266088
Start	32067016:32067016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>A
AA Mutation	p.Ala97Thr(p.A97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266088
Start	32084906:32084906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>A
AA Mutation	p.Val298Met(p.V298M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266088
Start	32081879:32081879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775315224
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Leu(p.S164L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266088
Start	32084446:32084446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145490212
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266088
Start	32084512:32084512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266088
Start	32086293:32086293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266088
Start	32086269:32086269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC5A1

No Mutation Annotation!