Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARHGAP32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128974466:128974466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200378366
CDS Mutation	c.2689C>T
AA Mutation	p.Arg897Trp(p.R897W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	129066789:129066789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>A
AA Mutation	p.Arg190Gln(p.R190Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128974222:128974222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765032782
CDS Mutation	c.2933A>G
AA Mutation	p.Asp978Gly(p.D978G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128973163:128973163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746571955
CDS Mutation	c.3301G>A
AA Mutation	p.Asp1101Asn(p.D1101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128970987:128970987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4184T>C
AA Mutation	p.Leu1395Pro(p.L1395P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128986580:128986580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345T>G
AA Mutation	p.Tyr449Asp(p.Y449D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128969892:128969892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550791905
CDS Mutation	c.5279G>A
AA Mutation	p.Arg1760His(p.R1760H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	129066828:129066828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371255312
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	129093653:129093653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770485511
CDS Mutation	c.457G>C
AA Mutation	p.Glu153Gln(p.E153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128976611:128976611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766918157
CDS Mutation	c.2104C>T
AA Mutation	p.Arg702Cys(p.R702C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310343
Start	128981418:128981418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736C>T
AA Mutation	p.Ala579Val(p.A579V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128976610:128976610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149060649
CDS Mutation	c.2105G>A
AA Mutation	p.Arg702His(p.R702H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128970048:128970048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5123C>T
AA Mutation	p.Ala1708Val(p.A1708V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128998341:128998341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1131C>A
AA Mutation	p.His377Gln(p.H377Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128970237:128970237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758198053
CDS Mutation	c.4934G>A
AA Mutation	p.Arg1645Gln(p.R1645Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	129064888:129064888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764660671
CDS Mutation	c.673A>G
AA Mutation	p.Ile225Val(p.I225V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	129164410:129164410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.134T>C
AA Mutation	p.Val45Ala(p.V45A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128980696:128980696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	129064859:129064859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128970497:128970497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4674G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128969288:128969288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5883A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128980636:128980636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751293823
CDS Mutation	c.1851G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128968991:128968991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6180C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128972696:128972696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3768C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	129123503:129123503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771908494
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128986665:128986665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	129093663:129093663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.447T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310343
Start	128981862:128981862(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1559delA
AA Mutation	p.Asn520IlefsTer2(p.N520Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310343
Start	128998459:128998459(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1013delA
AA Mutation	p.Lys338SerfsTer13(p.K338Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310343
Start	128986015:128986015(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1472delC
AA Mutation	p.Pro491HisfsTer10(p.P491Hfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000310343
Start	128972566:128972567(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3897_3898insTATATTTCATCT
AA Mutation	p.Thr1299_His1300insTyrIleSerSer(p.T1299_H1300insYISS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000310343
Start	128986664:128986665(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1260_1261insAAA
AA Mutation	p.His420_Glu421insLys(p.H420_E421insK)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128978826:128978826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141414658
CDS Mutation	c.2024G>A
AA Mutation	p.Arg675Gln(p.R675Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128998426:128998426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046T>C
AA Mutation	p.Phe349Ser(p.F349S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	129164356:129164356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188G>A
AA Mutation	p.Arg63Gln(p.R63Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310343
Start	128972707:128972707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768865360
CDS Mutation	c.3757G>A
AA Mutation	p.Glu1253Lys(p.E1253K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128974494:128974494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2661C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128969096:128969096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6075C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310343
Start	128974476:128974476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537107666
CDS Mutation	c.2679G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310343
Start	128974355:128974355(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2800delG
AA Mutation	p.Ala934HisfsTer23(p.A934Hfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript