Colon Cancer: Gene >> SLC1A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542575
Start	46777077:46777077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144030682
CDS Mutation	c.1286C>T
AA Mutation	p.Ala429Val(p.A429V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000542575
Start	46777095:46777095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767653184
CDS Mutation	c.1268C>T
AA Mutation	p.Ala423Val(p.A423V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000542575
Start	46777398:46777398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066A>G
AA Mutation	p.Thr356Ala(p.T356A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000542575
Start	46778744:46778744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749537352
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000542575
Start	46782470:46782470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748645826
CDS Mutation	c.737G>A
AA Mutation	p.Arg246Gln(p.R246Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000542575
Start	46787437:46787438(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.528dupC
AA Mutation	p.Ser177GlnfsTer33(p.S177Qfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC1A5

No Mutation Annotation!