Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GOT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99397629:99397629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387Gln(p.R387Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370508
Start	99406139:99406139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>A
AA Mutation	p.Glu179Lys(p.E179K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99403830:99403830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687C>A
AA Mutation	p.Phe229Leu(p.F229L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99397617:99397617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172G>A
AA Mutation	p.Ser391Asn(p.S391N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99420671:99420671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253T>G
AA Mutation	p.Ser85Ala(p.S85A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370508
Start	99402650:99402650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370508
Start	99403570:99403570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370508
Start	99403734:99403734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370508
Start	99402674:99402674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370508
Start	99406824:99406824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.326delG
AA Mutation	p.Gly109GlufsTer12(p.G109Efs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GOT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99397629:99397629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387Gln(p.R387Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99403514:99403514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769200718
CDS Mutation	c.914G>A
AA Mutation	p.Arg305Gln(p.R305Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99420799:99420799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370508
Start	99403829:99403829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772704095
CDS Mutation	c.688G>A
AA Mutation	p.Ala230Thr(p.A230T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370508
Start	99405789:99405789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139505253
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370508
Start	99406760:99406760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000370508
Start	99403599:99403599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829G>T
AA Mutation	p.Glu277Ter(p.E277*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript