Colon Cancer: Gene >> CAGE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7385869:7385869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Glu67Lys(p.E67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7374008:7374008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Ala271Thr(p.A271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000512086
Start	7373073:7373073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746G>T
AA Mutation	p.Lys582Asn(p.K582N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7373284:7373284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1535T>G
AA Mutation	p.Leu512Trp(p.L512W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7387027:7387027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147T>G
AA Mutation	p.His49Gln(p.H49Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7373490:7373490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329A>C
AA Mutation	p.Lys443Asn(p.K443N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000512086
Start	7374003:7374003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000512086
Start	7378764:7378764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778175256
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000512086
Start	7373094:7373094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1725C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000512086
Start	7378983:7378983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000512086
Start	7379009:7379009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295G>T
AA Mutation	p.Glu99Ter(p.E99*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CAGE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7373225:7373225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594A>C
AA Mutation	p.Lys532Gln(p.K532Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7378847:7378847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>T
AA Mutation	p.Asp153Tyr(p.D153Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000512086
Start	7387131:7387131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>T
AA Mutation	p.Pro15Ser(p.P15S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000512086
Start	7329885:7329885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2256A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000512086
Start	7373804:7373804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015G>T
AA Mutation	p.Glu339Ter(p.E339*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript