Colon Cancer: Gene >> JUP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41767422:41767422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866C>T
AA Mutation	p.Thr289Ile(p.T289I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41755877:41755877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200690479
CDS Mutation	c.2105G>A
AA Mutation	p.Arg702His(p.R702H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41757528:41757528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727504778
CDS Mutation	c.1933G>A
AA Mutation	p.Ala645Thr(p.A645T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41769152:41769152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782435477
CDS Mutation	c.524C>T
AA Mutation	p.Ser175Leu(p.S175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41769537:41769537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349G>A
AA Mutation	p.Ala117Thr(p.A117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41769549:41769549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>A
AA Mutation	p.Leu113Met(p.L113M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41769086:41769086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590G>A
AA Mutation	p.Ser197Asn(p.S197N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310706
Start	41758716:41758716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652C>T
AA Mutation	p.Thr551Met(p.T551M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41757473:41757473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1988G>A
AA Mutation	p.Arg663His(p.R663H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41757703:41757703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1855G>A
AA Mutation	p.Asp619Asn(p.D619N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41765039:41765039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938A>G
AA Mutation	p.Gln313Arg(p.Q313R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41758760:41758760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608G>T
AA Mutation	p.Gln536His(p.Q536H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41769516:41769516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370A>G
AA Mutation	p.Lys124Glu(p.K124E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310706
Start	41763124:41763124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555082435
CDS Mutation	c.1356G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310706
Start	41767511:41767511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34890640
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310706
Start	41757736:41757736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782661058
CDS Mutation	c.1822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000310706
Start	41758503:41758503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669G>T
AA Mutation	p.Glu557Ter(p.E557*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> JUP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41769474:41769474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150245906
CDS Mutation	c.412G>A
AA Mutation	p.Glu138Lys(p.E138K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310706
Start	41771788:41771788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>A
AA Mutation	p.Asp23Asn(p.D23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310706
Start	41757529:41757529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201704572
CDS Mutation	c.1932C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310706
Start	41763271:41763271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1209T>C
Mutation Classification	Silent
Feature Type	Transcript