Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARHGAP11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32633105:32633105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232G>A
AA Mutation	p.Cys411Tyr(p.C411Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32637226:32637226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2453C>A
AA Mutation	p.Ser818Tyr(p.S818Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32636884:32636884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2111A>G
AA Mutation	p.His704Arg(p.H704R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32623550:32623550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755147180
CDS Mutation	c.259C>T
AA Mutation	p.Arg87Trp(p.R87W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32637297:32637297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752534483
CDS Mutation	c.2524G>A
AA Mutation	p.Val842Ile(p.V842I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32633090:32633090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217C>T
AA Mutation	p.Ala406Val(p.A406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361627
Start	32628802:32628802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937G>C
AA Mutation	p.Ala313Pro(p.A313P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32636641:32636641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1868A>G
AA Mutation	p.Asn623Ser(p.N623S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32636922:32636922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2149T>G
AA Mutation	p.Phe717Val(p.F717V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32624227:32624227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352G>A
AA Mutation	p.Ala118Thr(p.A118T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32624397:32624397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522C>A
AA Mutation	p.Phe174Leu(p.F174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32634003:32634003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760030538
CDS Mutation	c.1306C>T
AA Mutation	p.Arg436Cys(p.R436C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361627
Start	32623537:32623537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140578993
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361627
Start	32636672:32636672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1899T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361627
Start	32629722:32629722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361627
Start	32628777:32628777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.912T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361627
Start	32624245:32624245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.375delT
AA Mutation	p.Phe125LeufsTer18(p.F125Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361627
Start	32636653:32636654(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1884dupA
AA Mutation	p.Leu629IlefsTer3(p.L629Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361627
Start	32624244:32624245(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.375dupT
AA Mutation	p.Arg126Ter(p.R126*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361627
Start	32636708:32636709(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1935_1936insCTTTC
AA Mutation	p.Thr646LeufsTer6(p.T646Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361627
Start	32623589:32623589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32637553:32637553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2780C>G
AA Mutation	p.Ser927Cys(p.S927C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32625543:32625543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772C>A
AA Mutation	p.Leu258Ile(p.L258I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32624420:32624420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545C>A
AA Mutation	p.Ser182Tyr(p.S182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361627
Start	32628755:32628755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890T>G
AA Mutation	p.Phe297Cys(p.F297C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361627
Start	32632986:32632986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138524535
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361627
Start	32616280:32616280(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.69delG
AA Mutation	p.Lys24ArgfsTer19(p.K24Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000361627
Start	32637529:32637529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2756C>A
AA Mutation	p.Ser919Ter(p.S919*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript