Colon Cancer: Gene >> OTULIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284274
Start	14681509:14681509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Cys(p.R124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284274
Start	14692905:14692905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Trp(p.R306W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284274
Start	14681537:14681537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Ala133Val(p.A133V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284274
Start	14692951:14692951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962C>G
AA Mutation	p.Thr321Ser(p.T321S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284274
Start	14678762:14678762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373661896
CDS Mutation	c.311C>T
AA Mutation	p.Thr104Met(p.T104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284274
Start	14692904:14692904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529302095
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284274
Start	14693027:14693027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284274
Start	14681577:14681577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284274
Start	14681541:14681541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000284274
Start	14673688:14673688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Glu67Ter(p.E67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000284274
Start	14687622:14687623(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.570_571insATAAAGAAGTGTTAACAT
AA Mutation	p.Glu190_Ser191insIleLysLysCysTerHis(p.E190_S191insIKKC*H)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OTULIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284274
Start	14687602:14687602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550C>A
AA Mutation	p.Leu184Met(p.L184M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000284274
Start	14673688:14673688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Glu67Ter(p.E67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript