Colon Cancer: Gene >> GRM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786474:86786474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>A
AA Mutation	p.Glu228Lys(p.E228K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786429:86786429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>A
AA Mutation	p.Val213Met(p.V213M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86765290:86765290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267601603
CDS Mutation	c.145G>A
AA Mutation	p.Glu49Lys(p.E49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86787018:86787018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409His(p.R409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86839071:86839071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1557G>T
AA Mutation	p.Lys519Asn(p.K519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86839543:86839543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563221454
CDS Mutation	c.2029G>A
AA Mutation	p.Ala677Thr(p.A677T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86765225:86765225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80A>T
AA Mutation	p.Asn27Ile(p.N27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786832:86786832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786903:86786903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Cys(p.R371C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86864315:86864315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2600A>C
AA Mutation	p.Asn867Thr(p.N867T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786654:86786654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.862G>A
AA Mutation	p.Ala288Thr(p.A288T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786825:86786825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033A>C
AA Mutation	p.Asn345His(p.N345H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786826:86786826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034A>T
AA Mutation	p.Asn345Ile(p.N345I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786706:86786706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914C>T
AA Mutation	p.Ala305Val(p.A305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86839517:86839517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755884573
CDS Mutation	c.2003G>A
AA Mutation	p.Arg668His(p.R668H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86850395:86850395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2417C>A
AA Mutation	p.Ser806Tyr(p.S806Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786930:86786930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138G>A
AA Mutation	p.Asp380Asn(p.D380N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86839813:86839813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267601607
CDS Mutation	c.2299G>A
AA Mutation	p.Glu767Lys(p.E767K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786870:86786870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078C>A
AA Mutation	p.Gln360Lys(p.Q360K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786473:86786473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786629:86786629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86765550:86765550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86839776:86839776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368293077
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786560:86786560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786362:86786362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754123274
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786791:86786791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786749:86786749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86765160:86765160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786746:86786746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000361669
Start	86838907:86838907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393C>T
AA Mutation	p.Arg465Ter(p.R465*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361669
Start	86787099:86787100(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1307_1308insCGTA
AA Mutation	p.Lys437ValfsTer13(p.K437Vfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GRM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786339:86786339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Cys(p.R183C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86786496:86786496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704G>A
AA Mutation	p.Arg235His(p.R235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86765290:86765290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267601603
CDS Mutation	c.145G>A
AA Mutation	p.Glu49Lys(p.E49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86864302:86864302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2587C>T
AA Mutation	p.Pro863Ser(p.P863S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86839444:86839444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777582336
CDS Mutation	c.1930C>T
AA Mutation	p.Arg644Cys(p.R644C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86787108:86787108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316A>T
AA Mutation	p.Asn439Ile(p.N439I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86765230:86765230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>A
AA Mutation	p.Leu29Ile(p.L29I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361669
Start	86839789:86839789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2275C>T
AA Mutation	p.Arg759Trp(p.R759W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361669
Start	86786791:86786791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript