Colon Cancer: Gene >> SLC5A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17883956:17883956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436C>T
AA Mutation	p.Ser479Leu(p.S479L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17874162:17874162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382G>A
AA Mutation	p.Ala128Thr(p.A128T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17872351:17872351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32C>T
AA Mutation	p.Thr11Ile(p.T11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17890936:17890936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570968775
CDS Mutation	c.1702G>A
AA Mutation	p.Ala568Thr(p.A568T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17875965:17875965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557C>A
AA Mutation	p.Ala186Asp(p.A186D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17883714:17883714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276C>T
AA Mutation	p.Pro426Ser(p.P426S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17872399:17872399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>T
AA Mutation	p.Ser27Phe(p.S27F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17883696:17883696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258A>G
AA Mutation	p.Met420Val(p.M420V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17890939:17890939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201835225
CDS Mutation	c.1705C>T
AA Mutation	p.Arg569Trp(p.R569W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222248
Start	17877816:17877816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148887708
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222248
Start	17893825:17893825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1884delC
AA Mutation	p.Cys629ValfsTer75(p.C629Vfs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC5A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222248
Start	17883965:17883965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776726081
CDS Mutation	c.1445G>A
AA Mutation	p.Arg482His(p.R482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222248
Start	17882020:17882020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222248
Start	17880894:17880894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222248
Start	17888343:17888343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757661931
CDS Mutation	c.1539C>T
Mutation Classification	Silent
Feature Type	Transcript