Colon Cancer: Gene >> SLC28A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84944619:84944619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717C>T
AA Mutation	p.Leu573Phe(p.L573F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84895091:84895091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>T
AA Mutation	p.Gln143His(p.Q143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84905619:84905619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684C>A
AA Mutation	p.Phe228Leu(p.F228L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84887836:84887836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78600895
CDS Mutation	c.76G>C
AA Mutation	p.Ala26Pro(p.A26P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84888836:84888836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201974180
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84935096:84935096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182952101
CDS Mutation	c.1285G>A
AA Mutation	p.Ala429Thr(p.A429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286749
Start	84935494:84935494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286749
Start	84904199:84904199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286749
Start	84944582:84944582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1680A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286749
Start	84923993:84923993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286749
Start	84924094:84924107(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1067_1080delCCTACATCTCCTTT
AA Mutation	p.Ala356GlyfsTer35(p.A356Gfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286749
Start	84924009:84924009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.984delC
AA Mutation	p.Tyr329ThrfsTer5(p.Y329Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC28A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84888822:84888822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147C>A
AA Mutation	p.Ser49Arg(p.S49R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84935190:84935190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1379T>A
AA Mutation	p.Phe460Tyr(p.F460Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286749
Start	84935331:84935331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765719750
CDS Mutation	c.1394C>T
AA Mutation	p.Ser465Phe(p.S465F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286749
Start	84943507:84943507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000286749
Start	84890504:84890504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564042221
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Ter(p.R83*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000286749
Start	84895077:84895078(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.417_418insATT
AA Mutation	p.Phe139_Leu140insIle(p.F139_L140insI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript