Colon Cancer: Gene >> CNTN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205058321:205058321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356C>T
AA Mutation	p.Thr119Ile(p.T119I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205061267:205061267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Cys(p.R274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205069839:205069839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2209G>A
AA Mutation	p.Glu737Lys(p.E737K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205059140:205059140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Cys(p.R182C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205064351:205064351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548252200
CDS Mutation	c.1270G>A
AA Mutation	p.Val424Met(p.V424M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205072064:205072064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775579054
CDS Mutation	c.2662G>A
AA Mutation	p.Val888Met(p.V888M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205073084:205073084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767209651
CDS Mutation	c.2861A>T
AA Mutation	p.Asp954Val(p.D954V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205073688:205073688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764275222
CDS Mutation	c.3046C>T
AA Mutation	p.Arg1016Cys(p.R1016C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205062443:205062443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538644037
CDS Mutation	c.1114C>T
AA Mutation	p.Arg372Trp(p.R372W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205064667:205064667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436G>A
AA Mutation	p.Ser479Asn(p.S479N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205064408:205064408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765367852
CDS Mutation	c.1327C>T
AA Mutation	p.Arg443Trp(p.R443W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205061943:205061943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052C>G
AA Mutation	p.Ala351Gly(p.A351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205061966:205061966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371816961
CDS Mutation	c.1075C>T
AA Mutation	p.Arg359Cys(p.R359C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205067236:205067236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139732381
CDS Mutation	c.2111G>A
AA Mutation	p.Arg704Gln(p.R704Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205065170:205065170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603G>A
AA Mutation	p.Asp535Asn(p.D535N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000331830
Start	205065811:205065811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718C>A
AA Mutation	p.Thr573Asn(p.T573N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205070012:205070012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772918166
CDS Mutation	c.2382C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205067126:205067126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205066445:205066445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1821G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205069838:205069838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2208G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205073190:205073190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766320758
CDS Mutation	c.2967C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205062544:205062544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764907069
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205071985:205071985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115143667
CDS Mutation	c.2583G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205059148:205059148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777614226
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331830
Start	205058238:205058238(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.278delG
AA Mutation	p.Gly93AlafsTer6(p.G93Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CNTN2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205072120:205072120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2718G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331830
Start	205059148:205059148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777614226
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript