Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GRIA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105612291:105612291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762714307
CDS Mutation	c.104G>A
AA Mutation	p.Arg35Gln(p.R35Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105924625:105924625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703T>G
AA Mutation	p.Phe568Cys(p.F568C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105974408:105974408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2508C>A
AA Mutation	p.Phe836Leu(p.F836L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105862152:105862152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>C
AA Mutation	p.Glu206Gln(p.E206Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105971957:105971957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761018528
CDS Mutation	c.2338G>A
AA Mutation	p.Val780Ile(p.V780I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105926842:105926842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949G>A
AA Mutation	p.Arg650Gln(p.R650Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000282499
Start	105887520:105887520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674T>C
AA Mutation	p.Ile225Thr(p.I225T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105924664:105924664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1742G>C
AA Mutation	p.Gly581Ala(p.G581A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105611023:105611023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26T>C
AA Mutation	p.Val9Ala(p.V9A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105933816:105933816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752319424
CDS Mutation	c.2141G>A
AA Mutation	p.Arg714His(p.R714H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105862099:105862099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563A>T
AA Mutation	p.Asn188Ile(p.N188I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105753067:105753067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763888983
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105924606:105924606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684T>A
AA Mutation	p.Leu562Ile(p.L562I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105926931:105926931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2038T>A
AA Mutation	p.Phe680Ile(p.F680I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105924675:105924675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1753C>T
AA Mutation	p.Pro585Ser(p.P585S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105924407:105924407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485G>T
AA Mutation	p.Glu495Asp(p.E495D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105903951:105903951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1023G>T
AA Mutation	p.Gln341His(p.Q341H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105918875:105918875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433A>G
AA Mutation	p.Asp478Gly(p.D478G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105926833:105926833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940C>T
AA Mutation	p.Thr647Met(p.T647M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105971989:105971989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762639803
CDS Mutation	c.2370C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105926894:105926894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2001T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105924605:105924605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1683C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105974405:105974405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2505G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105924653:105924653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105971935:105971935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105974426:105974426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2526A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105933784:105933784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105611051:105611051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769988493
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105862157:105862157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565566363
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282499
Start	105918746:105918746(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1306delA
AA Mutation	p.Met436CysfsTer13(p.M436Cfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000282499
Start	105903865:105903865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Ter(p.R313*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000282499
Start	105903949:105903949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021C>T
AA Mutation	p.Gln341Ter(p.Q341*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000282499
Start	105918904:105918904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462G>T
AA Mutation	p.Glu488Ter(p.E488*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GRIA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105612428:105612428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241A>C
AA Mutation	p.Asn81His(p.N81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105905201:105905201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353Gln(p.R353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105933843:105933843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144166964
CDS Mutation	c.2168C>T
AA Mutation	p.Ala723Val(p.A723V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105974317:105974317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2417C>T
AA Mutation	p.Thr806Met(p.T806M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105974434:105974434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2534A>C
AA Mutation	p.Lys845Thr(p.K845T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105753190:105753190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457T>A
AA Mutation	p.Cys153Ser(p.C153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105903914:105903914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>A
AA Mutation	p.Gly329Glu(p.G329E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105612335:105612335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148C>T
AA Mutation	p.Leu50Phe(p.L50F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105924402:105924402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480G>A
AA Mutation	p.Ala494Thr(p.A494T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105926755:105926755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1862G>A
AA Mutation	p.Arg621Gln(p.R621Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282499
Start	105933782:105933782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2107G>T
AA Mutation	p.Val703Leu(p.V703L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105887533:105887533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282499
Start	105979718:105979718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2688C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000282499
Start	105753001:105753001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268G>T
AA Mutation	p.Gly90Ter(p.G90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript