Colon Cancer: Gene >> LPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19956002:19956002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937C>A
AA Mutation	p.Leu313Met(p.L313M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19962136:19962136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344G>T
AA Mutation	p.Glu448Asp(p.E448D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19948203:19948203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557015233
CDS Mutation	c.112G>A
AA Mutation	p.Glu38Lys(p.E38K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19951796:19951796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>T
AA Mutation	p.Pro93Ser(p.P93S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19962215:19962215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423G>T
AA Mutation	p.Gly475Cys(p.G475C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19960974:19960974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213T>G
AA Mutation	p.Leu405Val(p.L405V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19954234:19954234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656G>A
AA Mutation	p.Arg219Gln(p.R219Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19959349:19959349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs298
CDS Mutation	c.1108G>A
AA Mutation	p.Val370Met(p.V370M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311322
Start	19955857:19955857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311322
Start	19939497:19939497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311322
Start	19951798:19951798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.282delA
AA Mutation	p.Lys94AsnfsTer78(p.K94Nfs*78)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000311322
Start	19951826:19951826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>T
AA Mutation	p.Glu103Ter(p.E103*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311322
Start	19955986:19955986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921G>T
AA Mutation	p.Lys307Asn(p.K307N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript