Colon Cancer: Gene >> SLC7A11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138219359:138219359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186693425
CDS Mutation	c.653C>T
AA Mutation	p.Thr218Met(p.T218M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138185234:138185234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>A
AA Mutation	p.Leu268Ile(p.L268I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138242053:138242053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763081007
CDS Mutation	c.17T>C
AA Mutation	p.Val6Ala(p.V6A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138185182:138185182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854A>T
AA Mutation	p.Asn285Ile(p.N285I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138219312:138219312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554325259
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Trp(p.R234W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138241903:138241903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167C>T
AA Mutation	p.Thr56Ile(p.T56I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138179273:138179273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771913516
CDS Mutation	c.1388C>T
AA Mutation	p.Ala463Val(p.A463V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138236364:138236364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365C>G
AA Mutation	p.Pro122Arg(p.P122R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138183280:138183280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941A>C
AA Mutation	p.Asn314Thr(p.N314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000280612
Start	138219363:138219363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>T
AA Mutation	p.Gln217Ter(p.Q217*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC7A11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138241846:138241846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>A
AA Mutation	p.Ser75Asn(p.S75N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138179265:138179265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757026554
CDS Mutation	c.1396C>A
AA Mutation	p.Leu466Ile(p.L466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280612
Start	138242015:138242015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55A>C
AA Mutation	p.Asn19His(p.N19H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript