Colon Cancer: Gene >> LIPE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42405552:42405552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2375C>T
AA Mutation	p.Thr792Met(p.T792M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42410434:42410434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757895823
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431His(p.R431H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42407619:42407619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1829T>C
AA Mutation	p.Leu610Pro(p.L610P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42408026:42408026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371540113
CDS Mutation	c.1606G>A
AA Mutation	p.Val536Met(p.V536M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42407285:42407285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2026G>A
AA Mutation	p.Ala676Thr(p.A676T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42402890:42402890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752221161
CDS Mutation	c.2684C>T
AA Mutation	p.Ser895Leu(p.S895L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42426758:42426758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392T>C
AA Mutation	p.Leu131Ser(p.L131S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42401961:42401961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3082A>G
AA Mutation	p.Thr1028Ala(p.T1028A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42427107:42427107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>T
AA Mutation	p.Pro15Ser(p.P15S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42426888:42426888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262C>A
AA Mutation	p.Leu88Ile(p.L88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42427019:42427019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131G>T
AA Mutation	p.Gly44Val(p.G44V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42405498:42405498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150433777
CDS Mutation	c.2429G>A
AA Mutation	p.Arg810Gln(p.R810Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42406272:42406272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2254G>A
AA Mutation	p.Ala752Thr(p.A752T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42407696:42407696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770751198
CDS Mutation	c.1752G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42407699:42407699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1749C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42410799:42410799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42410388:42410388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370746342
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42426583:42426583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749453513
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42402766:42402766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2808C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42427042:42427042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000244289
Start	42427112:42427112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38G>A
AA Mutation	p.Trp13Ter(p.W13*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LIPE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42410363:42410363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750527152
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Trp(p.R455W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42406373:42406373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150484479
CDS Mutation	c.2153G>A
AA Mutation	p.Arg718Gln(p.R718Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244289
Start	42406265:42406265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261C>T
AA Mutation	p.Pro754Leu(p.P754L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244289
Start	42426862:42426862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript