Colon Cancer: Gene >> SOX11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693968:5693968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247A>G
AA Mutation	p.Tyr416Cys(p.Y416C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693409:5693409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.688G>A
AA Mutation	p.Asp230Asn(p.D230N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693031:5693031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Trp(p.R104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693019:5693019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Trp(p.R100W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693160:5693160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775298170
CDS Mutation	c.439G>A
AA Mutation	p.Gly147Ser(p.G147S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5692768:5692768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Arg16Gln(p.R16Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5692804:5692804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83C>T
AA Mutation	p.Ala28Val(p.A28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5694007:5694007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286G>C
AA Mutation	p.Trp429Ser(p.W429S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5692794:5692794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693923:5693923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1202C>T
AA Mutation	p.Ser401Leu(p.S401L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5692768:5692768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47G>T
AA Mutation	p.Arg16Leu(p.R16L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693128:5693128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407A>C
AA Mutation	p.Gln136Pro(p.Q136P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693064:5693064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>A
AA Mutation	p.Asp115Asn(p.D115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693840:5693840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693153:5693153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693054:5693054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693063:5693063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693000:5693000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773377519
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693900:5693900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693031:5693031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693108:5693108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5693642:5693642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5692814:5692814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SOX11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322002
Start	5693913:5693913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192G>T
AA Mutation	p.Asp398Tyr(p.D398Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322002
Start	5692784:5692784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63G>C
Mutation Classification	Silent
Feature Type	Transcript