Colon Cancer: Gene >> SLC17A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62967412:62967412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223C>A
AA Mutation	p.Ala408Asp(p.A408D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62956862:62956862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157C>A
AA Mutation	p.Gln53Lys(p.Q53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370351
Start	62963585:62963585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62965147:62965147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564928264
CDS Mutation	c.926C>T
AA Mutation	p.Thr309Met(p.T309M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62960587:62960587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62962637:62962637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373281234
CDS Mutation	c.511G>A
AA Mutation	p.Gly171Arg(p.G171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370351
Start	62966719:62966719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201954865
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370351
Start	62957445:62957445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.266delG
AA Mutation	p.Gly89ValfsTer25(p.G89Vfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000370351
Start	62962675:62962675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549G>A
AA Mutation	p.Trp183Ter(p.W183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC17A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62965156:62965156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935A>C
AA Mutation	p.Lys312Thr(p.K312T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370351
Start	62965658:62965658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994A>T
AA Mutation	p.Thr332Ser(p.T332S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370351
Start	62965699:62965699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript