Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADCY9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114782:4114782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>A
AA Mutation	p.Val221Met(p.V221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114734:4114734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766756605
CDS Mutation	c.709G>A
AA Mutation	p.Val237Ile(p.V237I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3983427:3983427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2324C>T
AA Mutation	p.Ser775Phe(p.S775F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3983343:3983343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2408C>T
AA Mutation	p.Thr803Ile(p.T803I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3979253:3979253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375674603
CDS Mutation	c.2542G>A
AA Mutation	p.Val848Ile(p.V848I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294016
Start	3993407:3993407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988A>T
AA Mutation	p.Lys663Met(p.K663M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4115222:4115222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221G>A
AA Mutation	p.Arg74His(p.R74H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3992180:3992180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142301454
CDS Mutation	c.2173G>T
AA Mutation	p.Asp725Tyr(p.D725Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3966319:3966319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3518C>T
AA Mutation	p.Thr1173Met(p.T1173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3992273:3992273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2080G>A
AA Mutation	p.Glu694Lys(p.E694K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4113956:4113956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1487T>G
AA Mutation	p.Leu496Arg(p.L496R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3979166:3979166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144986362
CDS Mutation	c.2629G>A
AA Mutation	p.Ala877Thr(p.A877T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114566:4114566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Ala293Thr(p.A293T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114808:4114808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635G>A
AA Mutation	p.Arg212Gln(p.R212Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114296:4114296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Cys(p.R383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3993437:3993437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1958G>A
AA Mutation	p.Gly653Asp(p.G653D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4113813:4113813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772697228
CDS Mutation	c.1630G>A
AA Mutation	p.Glu544Lys(p.E544K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114758:4114758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685G>A
AA Mutation	p.Glu229Lys(p.E229K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114464:4114464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979A>C
AA Mutation	p.Lys327Gln(p.K327Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	4115113:4115113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758419751
CDS Mutation	c.330G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3974695:3974695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137924284
CDS Mutation	c.2844G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3966498:3966498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113410021
CDS Mutation	c.3339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3966009:3966009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199850891
CDS Mutation	c.3828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3977523:3977523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370804007
CDS Mutation	c.2787C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3966306:3966306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146365616
CDS Mutation	c.3531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3992331:3992331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112278827
CDS Mutation	c.2022C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3979173:3979173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2622G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3966177:3966177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3966525:3966525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759735634
CDS Mutation	c.3312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	4114024:4114024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765382815
CDS Mutation	c.1419C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294016
Start	4114588:4114588(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.855delG
AA Mutation	p.Leu286CysfsTer19(p.L286Cfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294016
Start	4114999:4114999(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.444delC
AA Mutation	p.Ala149ArgfsTer38(p.A149Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294016
Start	4114339:4114346(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1097_1104delCCAAGAAC
AA Mutation	p.Pro366GlnfsTer18(p.P366Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000294016
Start	4114269:4114269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174G>T
AA Mutation	p.Glu392Ter(p.E392*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADCY9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114491:4114491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952A>T
AA Mutation	p.Met318Leu(p.M318L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3965810:3965810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4027G>A
AA Mutation	p.Glu1343Lys(p.E1343K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3966375:3966375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3462C>A
AA Mutation	p.Asn1154Lys(p.N1154K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	4114758:4114758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685G>A
AA Mutation	p.Glu229Lys(p.E229K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294016
Start	3965834:3965834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374081146
CDS Mutation	c.4003G>A
AA Mutation	p.Glu1335Lys(p.E1335K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	4115068:4115068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148291399
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	3966498:3966498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113410021
CDS Mutation	c.3339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294016
Start	4115329:4115329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000294016
Start	4114269:4114269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174G>T
AA Mutation	p.Glu392Ter(p.E392*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript