Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ACIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23061517:23061517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3379C>T
AA Mutation	p.Pro1127Ser(p.P1127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23080407:23080407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102G>A
AA Mutation	p.Glu368Lys(p.E368K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23059153:23059153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4021C>T
AA Mutation	p.Arg1341Cys(p.R1341C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23059185:23059185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746023844
CDS Mutation	c.3989G>A
AA Mutation	p.Arg1330Gln(p.R1330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23061334:23061334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747738693
CDS Mutation	c.3562C>T
AA Mutation	p.Arg1188Cys(p.R1188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23080005:23080005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1504C>T
AA Mutation	p.Pro502Ser(p.P502S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23059156:23059156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4018C>T
AA Mutation	p.Arg1340Cys(p.R1340C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23064157:23064157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2717G>A
AA Mutation	p.Gly906Asp(p.G906D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23061552:23061552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3344G>T
AA Mutation	p.Arg1115Leu(p.R1115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23080513:23080513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996G>T
AA Mutation	p.Glu332Asp(p.E332D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23062496:23062496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3085A>G
AA Mutation	p.Lys1029Glu(p.K1029E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23061111:23061111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3672C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23061150:23061150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3633G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23062500:23062500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3081G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23059448:23059448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23062470:23062470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23080495:23080495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1014G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23080170:23080170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1339delG
AA Mutation	p.Ala447LeufsTer19(p.A447Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23061525:23061525(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3371delC
AA Mutation	p.Pro1124ArgfsTer106(p.P1124Rfs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000262710
Start	23080323:23080323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Ter(p.R396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23063514:23063515(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2831_2832dupCT
AA Mutation	p.Glu945LeufsTer13(p.E945Lfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23090569:23090569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443T>G
AA Mutation	p.Leu148Arg(p.L148R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23095108:23095108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179C>T
AA Mutation	p.Ala60Val(p.A60V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23066004:23066004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551895203
CDS Mutation	c.2444C>T
AA Mutation	p.Ser815Leu(p.S815L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262710
Start	23078822:23078822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779416155
CDS Mutation	c.2179C>T
AA Mutation	p.Arg727Trp(p.R727W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000262710
Start	23063538:23063538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2809G>T
AA Mutation	p.Glu937Ter(p.E937*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript