Colon Cancer: Gene >> GRIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137156775:137156775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778C>A
AA Mutation	p.Arg260Ser(p.R260S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137145805:137145805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473A>G
AA Mutation	p.Tyr158Cys(p.Y158C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137158657:137158657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1150G>A
AA Mutation	p.Gly384Arg(p.G384R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137139509:137139509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23C>T
AA Mutation	p.Thr8Met(p.T8M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137139593:137139593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107G>A
AA Mutation	p.Arg36Gln(p.R36Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137139726:137139726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240G>T
AA Mutation	p.Glu80Asp(p.E80D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137163597:137163597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2372C>T
AA Mutation	p.Thr791Met(p.T791M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137167469:137167469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2759G>A
AA Mutation	p.Arg920His(p.R920H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137156870:137156870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137139678:137139678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137142051:137142051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137139717:137139717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137156981:137156981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202240473
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137167470:137167470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2760C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000371561
Start	137139601:137139601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115G>T
AA Mutation	p.Glu39Ter(p.E39*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371561
Start	137163294:137163295(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2301dupC
AA Mutation	p.Trp768LeufsTer32(p.W768Lfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GRIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371561
Start	137156894:137156894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825G>T
AA Mutation	p.Lys275Asn(p.K275N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137163814:137163814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146086141
CDS Mutation	c.2499C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371561
Start	137163598:137163598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757177533
CDS Mutation	c.2373G>A
Mutation Classification	Silent
Feature Type	Transcript