Colon Cancer: Gene >> SLC5A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209836:101209836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13C>T
AA Mutation	p.Arg5Trp(p.R5W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101166567:101166567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453A>G
AA Mutation	p.Asn485Asp(p.N485D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209720:101209720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129G>T
AA Mutation	p.Lys43Asn(p.K43N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101166593:101166593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427A>G
AA Mutation	p.Asp476Gly(p.D476G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209752:101209752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97G>A
AA Mutation	p.Ala33Thr(p.A33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101166575:101166575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144331635
CDS Mutation	c.1445G>A
AA Mutation	p.Ser482Asn(p.S482N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209535:101209535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>A
AA Mutation	p.Pro105Gln(p.P105Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101190544:101190544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757T>C
AA Mutation	p.Trp253Arg(p.W253R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101195100:101195100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532A>T
AA Mutation	p.Thr178Ser(p.T178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101168131:101168131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150897103
CDS Mutation	c.1285G>A
AA Mutation	p.Ala429Thr(p.A429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209550:101209550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299C>T
AA Mutation	p.Ala100Val(p.A100V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101204535:101204535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555404331
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101204529:101204529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754809263
CDS Mutation	c.388T>C
AA Mutation	p.Cys130Arg(p.C130R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000536262
Start	101209819:101209819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000536262
Start	101187452:101187452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147034851
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC5A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209610:101209610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239G>A
AA Mutation	p.Arg80His(p.R80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101187451:101187451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377445681
CDS Mutation	c.898G>A
AA Mutation	p.Ala300Thr(p.A300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101209574:101209574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752445427
CDS Mutation	c.275A>G
AA Mutation	p.Tyr92Cys(p.Y92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101161995:101161995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609A>C
AA Mutation	p.Ile537Leu(p.I537L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101184201:101184201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Asp329Asn(p.D329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000536262
Start	101204535:101204535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555404331
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000536262
Start	101158284:101158284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675G>T
AA Mutation	p.Glu559Ter(p.E559*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript