Colon Cancer: Gene >> TLE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81585599:81585599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2034C>A
AA Mutation	p.Ser678Arg(p.S678R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81590955:81590955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1679C>T
AA Mutation	p.Ala560Val(p.A560V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81620523:81620523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629G>A
AA Mutation	p.Gly210Asp(p.G210D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81593141:81593141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465G>A
AA Mutation	p.Ala489Thr(p.A489T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81590886:81590886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748G>A
AA Mutation	p.Ser583Asn(p.S583N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81590974:81590974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660T>G
AA Mutation	p.Leu554Val(p.L554V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81611858:81611858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556195256
CDS Mutation	c.1165G>A
AA Mutation	p.Ala389Thr(p.A389T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81610227:81610227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324G>A
AA Mutation	p.Gly442Arg(p.G442R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376499
Start	81590944:81590944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1690C>T
AA Mutation	p.Pro564Ser(p.P564S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376499
Start	81591041:81591041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376499
Start	81685715:81685715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531243540
CDS Mutation	c.195T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376499
Start	81593199:81593199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545756552
CDS Mutation	c.1407C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376499
Start	81611850:81611850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150688751
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376499
Start	81590954:81590954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144048030
CDS Mutation	c.1680G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376499
Start	81585533:81585533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375370302
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000376499
Start	81685674:81685674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TLE1

No Mutation Annotation!