Colon Cancer: Gene >> SLC6A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000622186
Start	14472261:14472261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153A>G
AA Mutation	p.Thr385Ala(p.T385A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000622186
Start	14477275:14477275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763081342
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427His(p.R427H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000622186
Start	14468203:14468203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087G>T
AA Mutation	p.Ala363Ser(p.A363S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000622186
Start	14484946:14484946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200063855
CDS Mutation	c.1802G>A
AA Mutation	p.Arg601His(p.R601H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000622186
Start	14466580:14466580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797C>T
AA Mutation	p.Thr266Met(p.T266M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622186
Start	14447586:14447586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191620816
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622186
Start	14468151:14468151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622186
Start	14481727:14481727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622186
Start	14477327:14477327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1332G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622186
Start	14481712:14481712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000622186
Start	14477268:14477269(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1273_1274insCATTCT
AA Mutation	p.Gly425delinsAlaPheCys(p.G425delinsAFC)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A6

No Mutation Annotation!