Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARID4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58329542:58329542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Lys(p.R226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58301635:58301635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62G>A
AA Mutation	p.Arg21Gln(p.R21Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58364448:58364448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148135007
CDS Mutation	c.2359G>A
AA Mutation	p.Glu787Lys(p.E787K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58318770:58318770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414G>T
AA Mutation	p.Lys138Asn(p.K138N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58301619:58301619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46G>T
AA Mutation	p.Val16Phe(p.V16F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58365158:58365158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3069T>G
AA Mutation	p.Ser1023Arg(p.S1023R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355431
Start	58318776:58318776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373980107
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355431
Start	58364945:58364945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2856C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355431
Start	58366190:58366190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355431
Start	58371896:58371896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753619379
CDS Mutation	c.3681G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355431
Start	58360924:58360924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355431
Start	58301615:58301615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45562837
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58367001:58367001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3646delA
AA Mutation	p.Arg1216AspfsTer2(p.R1216Dfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58364688:58364688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2605delA
AA Mutation	p.Ile869Ter(p.I869*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58360917:58360917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1958delA
AA Mutation	p.Lys653ArgfsTer19(p.K653Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000355431
Start	58353755:58353755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1753C>T
AA Mutation	p.Arg585Ter(p.R585*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58347732:58347733(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1266dupA
AA Mutation	p.Asp423ArgfsTer24(p.D423Rfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58364418:58364419(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2335dupA
AA Mutation	p.Thr779AsnfsTer5(p.T779Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARID4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58367013:58367013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3654A>C
AA Mutation	p.Lys1218Asn(p.K1218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58306070:58306070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>A
AA Mutation	p.Ala78Thr(p.A78T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58364516:58364516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2427T>G
AA Mutation	p.Ile809Met(p.I809M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355431
Start	58364875:58364875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2786G>T
AA Mutation	p.Arg929Ile(p.R929I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58364419:58364419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2335delA
AA Mutation	p.Thr779GlnfsTer26(p.T779Qfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355431
Start	58351230:58351231(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1568dupA
AA Mutation	p.Asn523LysfsTer11(p.N523Kfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript