Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DLGAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34886096:34886096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576G>A
AA Mutation	p.Ala526Thr(p.A526T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34868638:34868638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748928423
CDS Mutation	c.2452C>T
AA Mutation	p.Arg818Cys(p.R818C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34900159:34900159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222G>T
AA Mutation	p.Asp408Tyr(p.D408Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904879:34904879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Cys(p.R169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34905115:34905115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269C>A
AA Mutation	p.Pro90His(p.P90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904585:34904585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799T>G
AA Mutation	p.Leu267Val(p.L267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34868905:34868905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142976280
CDS Mutation	c.2185C>T
AA Mutation	p.Arg729Cys(p.R729C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34905133:34905133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777868236
CDS Mutation	c.251G>T
AA Mutation	p.Gly84Val(p.G84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34905346:34905346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370097610
CDS Mutation	c.38G>A
AA Mutation	p.Arg13His(p.R13H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34900223:34900223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158G>T
AA Mutation	p.Glu386Asp(p.E386D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34885056:34885056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1922C>G
AA Mutation	p.Thr641Arg(p.T641R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34885057:34885057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1921A>G
AA Mutation	p.Thr641Ala(p.T641A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34867612:34867612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748658137
CDS Mutation	c.2501G>A
AA Mutation	p.Arg834His(p.R834H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34905361:34905361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23G>A
AA Mutation	p.Arg8Gln(p.R8Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34867560:34867560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2553C>A
AA Mutation	p.Phe851Leu(p.F851L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34868895:34868895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2195A>G
AA Mutation	p.His732Arg(p.H732R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000235180
Start	34867625:34867625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2488C>A
AA Mutation	p.Leu830Met(p.L830M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904834:34904834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550T>C
AA Mutation	p.Ser184Pro(p.S184P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34904718:34904718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34884983:34884983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1995C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34868630:34868630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139693504
CDS Mutation	c.2460G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34905174:34905174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748045752
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34868612:34868612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750597322
CDS Mutation	c.2478C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34905130:34905130(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766293453
CDS Mutation	c.254delG
AA Mutation	p.Gly85ValfsTer215(p.G85Vfs*215)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34900251:34900251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1130delG
AA Mutation	p.Gly377ValfsTer91(p.G377Vfs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34904545:34904545(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.839delC
AA Mutation	p.Pro280LeufsTer20(p.P280Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235180
Start	34905038:34905038(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.346delC
AA Mutation	p.Arg116AlafsTer184(p.R116Afs*184)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DLGAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34899712:34899712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762482299
CDS Mutation	c.1343G>A
AA Mutation	p.Arg448Gln(p.R448Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34886159:34886159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Trp(p.R505W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235180
Start	34904747:34904747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747689409
CDS Mutation	c.637G>A
AA Mutation	p.Gly213Ser(p.G213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235180
Start	34904469:34904469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781101151
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript