Colon Cancer: Gene >> SLC1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4564401:4564401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748031544
CDS Mutation	c.383C>T
AA Mutation	p.Ala128Val(p.A128V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4576583:4576583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>A
AA Mutation	p.Pro338His(p.P338H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262352
Start	4566049:4566049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443A>T
AA Mutation	p.Asn148Ile(p.N148I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4576104:4576104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979G>A
AA Mutation	p.Ala327Thr(p.A327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4585398:4585398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415A>C
AA Mutation	p.Gln472Pro(p.Q472P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4585387:4585387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404G>T
AA Mutation	p.Lys468Asn(p.K468N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4561472:4561472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752394755
CDS Mutation	c.256G>A
AA Mutation	p.Val86Ile(p.V86I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4585491:4585491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1508A>G
AA Mutation	p.Tyr503Cys(p.Y503C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262352
Start	4544619:4544619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763452671
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262352
Start	4544613:4544613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262352
Start	4576641:4576641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372708972
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262352
Start	4583078:4583078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1237delC
AA Mutation	p.Gln413ArgfsTer5(p.Q413Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262352
Start	4572313:4572313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.695delA
AA Mutation	p.Lys232ArgfsTer12(p.K232Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262352
Start	4566090:4566090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4576030:4576030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905C>T
AA Mutation	p.Pro302Leu(p.P302L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262352
Start	4544601:4544601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>A
AA Mutation	p.Ser42Arg(p.S42R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262352
Start	4585420:4585420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437C>A
Mutation Classification	Silent
Feature Type	Transcript