Colon Cancer: Gene >> LIPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58548366:58548366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845C>T
AA Mutation	p.Ser282Leu(p.S282L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58545958:58545958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776463699
CDS Mutation	c.791C>T
AA Mutation	p.Ala264Val(p.A264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58538463:58538463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>T
AA Mutation	p.Gln73His(p.Q73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58548399:58548399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878C>T
AA Mutation	p.Ala293Val(p.A293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000299022
Start	58538334:58538334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>T
AA Mutation	p.Glu30Asp(p.E30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58548338:58548338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>A
AA Mutation	p.Gln273Lys(p.Q273K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58545847:58545847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680A>G
AA Mutation	p.His227Arg(p.H227R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299022
Start	58542629:58542629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746964093
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299022
Start	58548367:58548367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762938418
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299022
Start	58538406:58538406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299022
Start	58542608:58542608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761213115
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000299022
Start	58568813:58568813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371396620
CDS Mutation	c.1486C>T
AA Mutation	p.Arg496Ter(p.R496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LIPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58548383:58548383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761575901
CDS Mutation	c.862G>A
AA Mutation	p.Asp288Asn(p.D288N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58568799:58568799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1472C>A
AA Mutation	p.Ser491Tyr(p.S491Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58545804:58545804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780399994
CDS Mutation	c.637G>T
AA Mutation	p.Asp213Tyr(p.D213Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299022
Start	58548425:58548425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904T>G
AA Mutation	p.Cys302Gly(p.C302G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299022
Start	58563565:58563565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770613137
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299022
Start	58563532:58563532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560051123
CDS Mutation	c.1197G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000299022
Start	58538437:58538437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369262181
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Ter(p.R65*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript