Colon Cancer: Gene >> SLC38A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55649217:55649217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1050T>G
AA Mutation	p.Phe350Leu(p.F350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55652719:55652719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762T>G
AA Mutation	p.Ile254Met(p.I254M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55672682:55672682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55626625:55626625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555T>A
AA Mutation	p.Phe519Ile(p.F519I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55645847:55645847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109T>G
AA Mutation	p.Phe370Cys(p.F370C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55664860:55664860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759238694
CDS Mutation	c.530C>T
AA Mutation	p.Ser177Leu(p.S177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318672
Start	55664720:55664720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670C>A
AA Mutation	p.Leu224Ile(p.L224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318672
Start	55669784:55669784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139575595
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318672
Start	55626500:55626500(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1680delT
AA Mutation	p.Phe560LeufsTer17(p.F560Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318672
Start	55652547:55652547(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.934delT
AA Mutation	p.Ser312GlnfsTer6(p.S312Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318672
Start	55645843:55645843(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1113delT
AA Mutation	p.Phe371LeufsTer10(p.F371Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC38A9

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000318672
Start	55664860:55664860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>A
AA Mutation	p.Ser177Ter(p.S177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript