Colon Cancer: Gene >> ACLY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41905546:41905546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979A>G
AA Mutation	p.Met327Val(p.M327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41893039:41893039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595C>A
AA Mutation	p.Pro532His(p.P532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000352035
Start	41901812:41901812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067G>A
AA Mutation	p.Gly356Asp(p.G356D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41901801:41901801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078G>A
AA Mutation	p.Ala360Thr(p.A360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41872124:41872124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2701G>A
AA Mutation	p.Gly901Arg(p.G901R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41869571:41869571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2954T>C
AA Mutation	p.Met985Thr(p.M985T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41913845:41913845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200879681
CDS Mutation	c.29C>T
AA Mutation	p.Thr10Met(p.T10M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41886227:41886227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565573136
CDS Mutation	c.1957C>T
AA Mutation	p.Arg653Cys(p.R653C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41907462:41907462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>T
AA Mutation	p.Gly243Trp(p.G243W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41907459:41907459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730C>T
AA Mutation	p.Arg244Trp(p.R244W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41886194:41886194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1990G>A
AA Mutation	p.Gly664Arg(p.G664R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41867820:41867820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3296T>C
AA Mutation	p.Met1099Thr(p.M1099T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41867833:41867833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3283C>A
AA Mutation	p.Leu1095Ile(p.L1095I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41897814:41897814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364C>A
AA Mutation	p.Ser455Tyr(p.S455Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41868754:41868754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3166G>A
AA Mutation	p.Ala1056Thr(p.A1056T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000352035
Start	41901756:41901756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188073019
CDS Mutation	c.1123A>G
AA Mutation	p.Ile375Val(p.I375V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352035
Start	41884268:41884268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140674334
CDS Mutation	c.2079G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352035
Start	41905635:41905635(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.890delG
AA Mutation	p.Gly297ValfsTer31(p.G297Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ACLY

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352035
Start	41869546:41869546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144346203
CDS Mutation	c.2979C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352035
Start	41907463:41907463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782400219
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352035
Start	41878145:41878145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2445G>A
Mutation Classification	Silent
Feature Type	Transcript