Colon Cancer: Gene >> SLC3A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62885205:62885205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751067361
CDS Mutation	c.1150G>A
AA Mutation	p.Asp384Asn(p.D384N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62888464:62888464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1664G>A
AA Mutation	p.Arg555His(p.R555H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62888655:62888655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855C>T
AA Mutation	p.His619Tyr(p.H619Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62882914:62882914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908G>A
AA Mutation	p.Arg303His(p.R303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62888638:62888638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374261898
CDS Mutation	c.1838G>A
AA Mutation	p.Arg613His(p.R613H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62888370:62888370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779207226
CDS Mutation	c.1570C>T
AA Mutation	p.Arg524Trp(p.R524W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62888400:62888400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753612198
CDS Mutation	c.1600C>T
AA Mutation	p.Arg534Cys(p.R534C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377890
Start	62888356:62888356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556T>C
AA Mutation	p.Leu519Pro(p.L519P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377890
Start	62888483:62888483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1683G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377890
Start	62882057:62882057(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.899delA
AA Mutation	p.Lys300ArgfsTer31(p.K300Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000377890
Start	62885513:62885513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351C>T
AA Mutation	p.Arg451Ter(p.R451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC3A2

No Mutation Annotation!