Colon Cancer: Gene >> GRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146159413:146159413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.766G>A
AA Mutation	p.Ala256Thr(p.A256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146434398:146434398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3187C>T
AA Mutation	p.Arg1063Trp(p.R1063W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029623:146029623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Cys(p.R36C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146434152:146434152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2941C>T
AA Mutation	p.Arg981Cys(p.R981C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399075:146399075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2036C>A
AA Mutation	p.Thr679Asn(p.T679N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029615:146029615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98C>T
AA Mutation	p.Ser33Leu(p.S33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399368:146399368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2329G>A
AA Mutation	p.Val777Met(p.V777M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029795:146029795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278C>T
AA Mutation	p.Pro93Leu(p.P93L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029697:146029697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>T
AA Mutation	p.Glu60Asp(p.E60D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146159470:146159470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Cys(p.R275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399434:146399434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2395C>A
AA Mutation	p.Leu799Ile(p.L799I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146434428:146434428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3217C>A
AA Mutation	p.Gln1073Lys(p.Q1073K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146159560:146159560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Cys(p.R305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399433:146399433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2394G>T
AA Mutation	p.Trp798Cys(p.W798C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146159471:146159471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553512718
CDS Mutation	c.824G>A
AA Mutation	p.Arg275His(p.R275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146304748:146304748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768125686
CDS Mutation	c.1088C>T
AA Mutation	p.Thr363Met(p.T363M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146433945:146433945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2734C>T
AA Mutation	p.Arg912Cys(p.R912C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146434080:146434080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2869G>A
AA Mutation	p.Val957Ile(p.V957I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146352303:146352303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240A>G
AA Mutation	p.Ile414Val(p.I414V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146386930:146386930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201399008
CDS Mutation	c.1643C>T
AA Mutation	p.Thr548Met(p.T548M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399494:146399494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2455G>T
AA Mutation	p.Val819Leu(p.V819L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146159440:146159440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>A
AA Mutation	p.Ala265Thr(p.A265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399623:146399623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584G>A
AA Mutation	p.Asp862Asn(p.D862N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029624:146029624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107G>A
AA Mutation	p.Arg36His(p.R36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399003:146399003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1964C>A
AA Mutation	p.Thr655Asn(p.T655N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434451:146434451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3240G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146029706:146029706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146399400:146399400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762664865
CDS Mutation	c.2361C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146398827:146398827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146029949:146029949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434079:146434079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2868C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434499:146434499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146159544:146159544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434394:146434394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3183G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434487:146434487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434433:146434433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146030198:146030198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148483275
CDS Mutation	c.681C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146399658:146399658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765450864
CDS Mutation	c.2619C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434395:146434395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3184C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146030006:146030006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282753
Start	146029958:146029958(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.446delC
AA Mutation	p.Pro149GlnfsTer11(p.P149Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282753
Start	146434251:146434251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3044delC
AA Mutation	p.Pro1015LeufsTer16(p.P1015Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146398813:146398813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112775415
CDS Mutation	c.1774G>A
AA Mutation	p.Glu592Lys(p.E592K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146352411:146352411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348C>G
AA Mutation	p.Leu450Val(p.L450V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146399170:146399170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2131T>C
AA Mutation	p.Ser711Pro(p.S711P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029834:146029834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>A
AA Mutation	p.Arg106Gln(p.R106Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282753
Start	146029976:146029976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459G>T
AA Mutation	p.Lys153Asn(p.K153N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146399373:146399373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138085475
CDS Mutation	c.2334C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434577:146434577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146434163:146434163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2952C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146029766:146029766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282753
Start	146399475:146399475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2436C>A
Mutation Classification	Silent
Feature Type	Transcript