Colon Cancer: Gene >> SFPQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35187047:35187047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940G>A
AA Mutation	p.Gly647Asp(p.G647D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35187235:35187235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Gln(p.R611Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35188076:35188076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571Gln(p.R571Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35190515:35190515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1398G>T
AA Mutation	p.Lys466Asn(p.K466N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35189192:35189192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606C>T
AA Mutation	p.Arg536Cys(p.R536C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35184565:35184565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371481157
CDS Mutation	c.2015C>T
AA Mutation	p.Ala672Val(p.A672V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35189336:35189336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462T>C
AA Mutation	p.Tyr488His(p.Y488H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35189333:35189333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465G>A
AA Mutation	p.Glu489Lys(p.E489K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35188047:35188047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Cys(p.R581C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35189270:35189270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528A>C
AA Mutation	p.Lys510Gln(p.K510Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SFPQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35187992:35187992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765938341
CDS Mutation	c.1796G>A
AA Mutation	p.Arg599Gln(p.R599Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35189258:35189258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540G>A
AA Mutation	p.Asp514Asn(p.D514N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357214
Start	35191351:35191351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007T>G
AA Mutation	p.Phe336Cys(p.F336C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript