Colon Cancer: Gene >> DNTT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96328827:96328827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110G>T
AA Mutation	p.Lys370Asn(p.K370N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96319356:96319356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756558035
CDS Mutation	c.473G>T
AA Mutation	p.Arg158Ile(p.R158I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96332512:96332512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275G>T
AA Mutation	p.Lys425Asn(p.K425N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96335964:96335964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433A>G
AA Mutation	p.Asp478Gly(p.D478G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96304553:96304553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756316751
CDS Mutation	c.56C>T
AA Mutation	p.Thr19Met(p.T19M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96318387:96318387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Ser80Leu(p.S80L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96335935:96335935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404G>T
AA Mutation	p.Lys468Asn(p.K468N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96332468:96332468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Cys(p.R411C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96318515:96318515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367C>T
AA Mutation	p.His123Tyr(p.H123Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371174
Start	96304554:96304554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777964414
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371174
Start	96319303:96319303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201827729
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371174
Start	96318448:96318448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000371174
Start	96328789:96328789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072G>T
AA Mutation	p.Glu358Ter(p.E358*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000371174
Start	96322711:96322711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369785092
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Ter(p.R245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DNTT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96335942:96335942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411C>A
AA Mutation	p.Leu471Met(p.L471M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96322712:96322712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734G>A
AA Mutation	p.Arg245Gln(p.R245Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371174
Start	96332512:96332512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275G>T
AA Mutation	p.Lys425Asn(p.K425N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371174
Start	96327574:96327574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771895179
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript