Colon Cancer: Gene >> SLC6A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30210542:30210542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1422C>A
AA Mutation	p.Phe474Leu(p.F474L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30203236:30203236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1754C>T
AA Mutation	p.Ser585Phe(p.S585F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30218133:30218133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683C>T
AA Mutation	p.Ala228Val(p.A228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30198472:30198472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142441982
CDS Mutation	c.1877G>A
AA Mutation	p.Arg626His(p.R626H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30218844:30218844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147306146
CDS Mutation	c.431G>A
AA Mutation	p.Arg144Gln(p.R144Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30210580:30210580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771843360
CDS Mutation	c.1384C>T
AA Mutation	p.Arg462Trp(p.R462W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261707
Start	30207780:30207780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1602G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261707
Start	30209195:30209195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777581886
CDS Mutation	c.1497C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261707
Start	30212744:30212744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148279474
CDS Mutation	c.1200C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261707
Start	30221629:30221629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261707
Start	30203246:30203247(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1743_1744delAG
AA Mutation	p.Ile581MetfsTer24(p.I581Mfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261707
Start	30216180:30216180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770779030
CDS Mutation	c.874C>A
AA Mutation	p.Leu292Ile(p.L292I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript