Colon Cancer: Gene >> TJP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69226155:69226155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190A>T
AA Mutation	p.Asp397Val(p.D397V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69237022:69237022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779161706
CDS Mutation	c.2065C>T
AA Mutation	p.Arg689Cys(p.R689C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69228072:69228072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149386335
CDS Mutation	c.1411C>T
AA Mutation	p.Pro471Ser(p.P471S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69251281:69251281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3238G>T
AA Mutation	p.Gly1080Cys(p.G1080C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69221364:69221364(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	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69227789:69227789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748959984
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412Gln(p.R412Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69225360:69225360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009C>A
AA Mutation	p.Leu337Met(p.L337M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69254328:69254328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3527G>A
AA Mutation	p.Arg1176His(p.R1176H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69237001:69237001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760622082
CDS Mutation	c.2044C>T
AA Mutation	p.Arg682Trp(p.R682W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69236091:69236091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1844G>A
AA Mutation	p.Cys615Tyr(p.C615Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69237893:69237893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195C>A
AA Mutation	p.Pro732His(p.P732H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69234498:69234498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1731A>C
AA Mutation	p.Glu577Asp(p.E577D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69220920:69220920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756272179
CDS Mutation	c.376G>A
AA Mutation	p.Ala126Thr(p.A126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69249403:69249403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150494393
CDS Mutation	c.2909G>A
AA Mutation	p.Arg970Gln(p.R970Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69216459:69216459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235C>A
AA Mutation	p.Leu79Ile(p.L79I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69228108:69228108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447C>A
AA Mutation	p.Pro483Thr(p.P483T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69238742:69238742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2308T>A
AA Mutation	p.Ser770Thr(p.S770T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69227812:69227812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199761505
CDS Mutation	c.1258C>T
AA Mutation	p.Arg420Cys(p.R420C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377245
Start	69221234:69221234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377245
Start	69240013:69240013(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776869985
CDS Mutation	c.2438delT
AA Mutation	p.Phe813SerfsTer12(p.F813Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377245
Start	69240120:69240120(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2545delA
AA Mutation	p.Thr849ArgfsTer12(p.T849Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377245
Start	69221074:69221074(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.534delG
AA Mutation	p.Arg179ValfsTer132(p.R179Vfs*132)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377245
Start	69212597:69212597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.113delA
AA Mutation	p.Lys38ArgfsTer105(p.K38Rfs*105)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377245
Start	69228107:69228107(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1451delC
AA Mutation	p.Pro484GlnfsTer30(p.P484Qfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000377245
Start	69238787:69238787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2353C>T
AA Mutation	p.Gln785Ter(p.Q785*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000377245
Start	69218258:69218258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241G>T
AA Mutation	p.Glu81Ter(p.E81*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000377245
Start	69248150:69248150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2806G>T
AA Mutation	p.Glu936Ter(p.E936*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000377245
Start	69218360:69218361(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.342+2dupT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TJP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377245
Start	69226050:69226050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085C>A
AA Mutation	p.Ser362Tyr(p.S362Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript