Colon Cancer: Gene >> SP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53382336:53382336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389G>A
AA Mutation	p.Gly130Asp(p.G130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53382648:53382648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701A>T
AA Mutation	p.Gln234Leu(p.Q234L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53383485:53383485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1538C>T
AA Mutation	p.Ala513Val(p.A513V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53382505:53382505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>T
AA Mutation	p.Gln186His(p.Q186H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53382956:53382956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>A
AA Mutation	p.Gly337Arg(p.G337R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53383429:53383429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482G>T
AA Mutation	p.Gln494His(p.Q494H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53382705:53382705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758T>C
AA Mutation	p.Val253Ala(p.V253A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327443
Start	53382148:53382148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327443
Start	53383318:53383318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327443
Start	53382627:53382627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680C>G
AA Mutation	p.Ala227Gly(p.A227G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000327443
Start	53382599:53382599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Ter(p.R218*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000327443
Start	53382203:53382203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256C>T
AA Mutation	p.Gln86Ter(p.Q86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript