Colon Cancer: Gene >> SLC6A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55656744:55656744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760211721
CDS Mutation	c.50C>T
AA Mutation	p.Ala17Val(p.A17V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55700232:55700232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144701163
CDS Mutation	c.1684G>A
AA Mutation	p.Ala562Thr(p.A562T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55700238:55700238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1690T>C
AA Mutation	p.Ser564Pro(p.S564P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55672076:55672076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Ser182Asn(p.S182N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55671964:55671964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55695321:55695321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs5565
CDS Mutation	c.1066G>A
AA Mutation	p.Val356Ile(p.V356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55699592:55699592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1528G>A
AA Mutation	p.Gly510Arg(p.G510R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55691979:55691979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845T>C
AA Mutation	p.Val282Ala(p.V282A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55685174:55685174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557196282
CDS Mutation	c.676G>A
AA Mutation	p.Gly226Arg(p.G226R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55656768:55656768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74T>C
AA Mutation	p.Leu25Pro(p.L25P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55685237:55685237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11568341
CDS Mutation	c.739G>A
AA Mutation	p.Val247Ile(p.V247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55700230:55700230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1682T>C
AA Mutation	p.Ile561Thr(p.I561T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55692036:55692036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147833183
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55701903:55701903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799T>C
AA Mutation	p.Leu600Pro(p.L600P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55656865:55656865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55691950:55691950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55697983:55697983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55685272:55685272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55672113:55672113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146377944
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55656814:55656814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753908637
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000379906
Start	55672071:55672071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540G>A
AA Mutation	p.Trp180Ter(p.W180*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55695333:55695333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078G>A
AA Mutation	p.Ala360Thr(p.A360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379906
Start	55669651:55669651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758931200
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Trp(p.R121W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55669581:55669581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749112583
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55656853:55656853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750613505
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55698004:55698004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379906
Start	55671999:55671999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769118691
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000379906
Start	55695366:55695366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1111G>T
AA Mutation	p.Glu371Ter(p.E371*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript