Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SYNM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99130646:99130646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2286G>T
AA Mutation	p.Glu762Asp(p.E762D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99129416:99129416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056A>C
AA Mutation	p.Glu352Asp(p.E352D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99132910:99132910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4550G>A
AA Mutation	p.Arg1517Lys(p.R1517K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99132385:99132385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4025C>G
AA Mutation	p.Thr1342Ser(p.T1342S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99131443:99131443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3083A>T
AA Mutation	p.Glu1028Val(p.E1028V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99132658:99132658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782239415
CDS Mutation	c.4298C>T
AA Mutation	p.Ala1433Val(p.A1433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99129961:99129961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601A>T
AA Mutation	p.Glu534Val(p.E534V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99130371:99130371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375383176
CDS Mutation	c.2011G>A
AA Mutation	p.Val671Met(p.V671M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99105761:99105761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Ala188Thr(p.A188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99132106:99132106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3746A>C
AA Mutation	p.Tyr1249Ser(p.Y1249S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99132441:99132441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4081G>A
AA Mutation	p.Gly1361Ser(p.G1361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99132839:99132839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4479G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99129614:99129614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782527382
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99129935:99129935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569566682
CDS Mutation	c.1575C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99130691:99130691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776015304
CDS Mutation	c.2331G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99131375:99131375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3015C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99131861:99131861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3501C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99129698:99129698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99131660:99131660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782771735
CDS Mutation	c.3300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99132737:99132737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141276249
CDS Mutation	c.4377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99130013:99130013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336292
Start	99130271:99130271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336292
Start	99130702:99130702(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2346delG
AA Mutation	p.Leu783TrpfsTer36(p.L783Wfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336292
Start	99130874:99130874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2517delC
AA Mutation	p.His842ThrfsTer47(p.H842Tfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000336292
Start	99131154:99131154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2794G>T
AA Mutation	p.Glu932Ter(p.E932*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000336292
Start	99126738:99126738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Glu318Ter(p.E318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000336292
Start	99129861:99129861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1501G>T
AA Mutation	p.Glu501Ter(p.E501*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SYNM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99130887:99130887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782563872
CDS Mutation	c.2527G>A
AA Mutation	p.Asp843Asn(p.D843N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99131310:99131310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369298488
CDS Mutation	c.2950G>A
AA Mutation	p.Val984Met(p.V984M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99113648:99113648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868T>G
AA Mutation	p.Trp290Gly(p.W290G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99131115:99131115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376246829
CDS Mutation	c.2755G>A
AA Mutation	p.Glu919Lys(p.E919K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336292
Start	99132736:99132736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782418930
CDS Mutation	c.4376C>T
AA Mutation	p.Ser1459Leu(p.S1459L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000336292
Start	99132516:99132516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4156G>T
AA Mutation	p.Glu1386Ter(p.E1386*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000336292
Start	99131136:99131136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2776G>T
AA Mutation	p.Glu926Ter(p.E926*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript