Colon Cancer: Gene >> SLC6A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1409773:1409773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780134296
CDS Mutation	c.1346C>T
AA Mutation	p.Thr449Met(p.T449M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1443130:1443130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>T
AA Mutation	p.Ala23Val(p.A23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1406225:1406225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760024050
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521Gln(p.R521Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1403013:1403013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28364997
CDS Mutation	c.1676C>T
AA Mutation	p.Ala559Val(p.A559V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000270349
Start	1422012:1422012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753109365
CDS Mutation	c.656G>A
AA Mutation	p.Arg219His(p.R219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1402962:1402962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727C>A
AA Mutation	p.Ala576Glu(p.A576E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1443138:1443138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60G>T
AA Mutation	p.Glu20Asp(p.E20D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270349
Start	1411252:1411252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367952238
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270349
Start	1409045:1409045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764518683
CDS Mutation	c.1479C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270349
Start	1422008:1422008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs118141909
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270349
Start	1414698:1414698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1149C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270349
Start	1411246:1411246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000270349
Start	1416197:1416197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>A
AA Mutation	p.Trp311Ter(p.W311*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270349
Start	1414739:1414740(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1107dupG
AA Mutation	p.Tyr370ValfsTer68(p.Y370Vfs*68)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1403013:1403013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28364997
CDS Mutation	c.1676C>T
AA Mutation	p.Ala559Val(p.A559V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1402953:1402953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736A>C
AA Mutation	p.Lys579Thr(p.K579T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1406226:1406226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs431905516
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Trp(p.R521W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270349
Start	1443165:1443165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>A
AA Mutation	p.Met11Ile(p.M11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript