Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CNTN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74301757:74301757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1835C>A
AA Mutation	p.Thr612Lys(p.T612K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74369240:74369240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895G>T
AA Mutation	p.Ala299Ser(p.A299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74295168:74295168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2470A>G
AA Mutation	p.Asn824Asp(p.N824D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74361922:74361922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1332G>T
AA Mutation	p.Lys444Asn(p.K444N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74365583:74365583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1066G>T
AA Mutation	p.Ala356Ser(p.A356S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74499662:74499662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179A>G
AA Mutation	p.Tyr60Cys(p.Y60C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74267331:74267331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2752A>G
AA Mutation	p.Lys918Glu(p.K918E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263665
Start	74297957:74297957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2401G>A
AA Mutation	p.Glu801Lys(p.E801K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74369204:74369204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263665
Start	74285305:74285305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2704C>T
AA Mutation	p.Pro902Ser(p.P902S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74365653:74365653(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	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74361914:74361914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1340A>G
AA Mutation	p.Asp447Gly(p.D447G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74371363:74371363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752936529
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Leu(p.S164L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74499706:74499706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135A>T
AA Mutation	p.Lys45Asn(p.K45N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74264498:74264498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2990T>C
AA Mutation	p.Met997Thr(p.M997T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74297961:74297961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2397A>C
AA Mutation	p.Glu799Asp(p.E799D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74297996:74297996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2362C>T
AA Mutation	p.Pro788Ser(p.P788S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74364474:74364474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74266632:74266632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2835C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74301522:74301522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111626135
CDS Mutation	c.1971G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74424888:74424888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746345698
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74267368:74267368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2715G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74285408:74285408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2601G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74424936:74424936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000263665
Start	74499771:74499771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>T
AA Mutation	p.Gln24Ter(p.Q24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263665
Start	74302722:74302723(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1753_1754insCT
AA Mutation	p.Ser585ThrfsTer10(p.S585Tfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263665
Start	74302724:74302725(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1751_1752insTATTTCC
AA Mutation	p.Ser585IlefsTer9(p.S585Ifs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CNTN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74334907:74334907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496C>T
AA Mutation	p.Pro499Leu(p.P499L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74424895:74424895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775718393
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74334846:74334846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1557G>T
AA Mutation	p.Leu519Phe(p.L519F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74297969:74297969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2389T>A
AA Mutation	p.Ser797Thr(p.S797T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74364531:74364531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>T
AA Mutation	p.Met383Ile(p.M383I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74301473:74301473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2020C>T
AA Mutation	p.Arg674Trp(p.R674W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript