Colon Cancer: Gene >> CEL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133062033:133062033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40C>A
AA Mutation	p.Leu14Ile(p.L14I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133071744:133071744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2251C>T
AA Mutation	p.Pro751Ser(p.P751S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133071666:133071666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202034862
CDS Mutation	c.2173G>C
AA Mutation	p.Ala725Pro(p.A725P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133067152:133067152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851C>T
AA Mutation	p.Thr284Ile(p.T284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133067133:133067133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Ala278Thr(p.A278T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133064467:133064467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>T
AA Mutation	p.Gly47Cys(p.G47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133064756:133064756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343A>G
AA Mutation	p.Lys115Glu(p.K115E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133065057:133065057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201336247
CDS Mutation	c.367G>A
AA Mutation	p.Val123Ile(p.V123I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133068757:133068757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133069143:133069143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1179C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133065056:133065056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185977842
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133068796:133068796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201061188
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133064409:133064409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771328351
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133070563:133070563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554390636
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133065140:133065140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133066624:133066624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762719603
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372080
Start	133065206:133065206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372080
Start	133071678:133071678(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2190delC
AA Mutation	p.Thr731ArgfsTer30(p.T731Rfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372080
Start	133071667:133071667(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2180delC
AA Mutation	p.Pro727LeufsTer34(p.P727Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CEL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133068840:133068840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751226585
CDS Mutation	c.1073G>A
AA Mutation	p.Gly358Asp(p.G358D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372080
Start	133066868:133066868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746040301
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Trp(p.R237W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript