Colon Cancer: Gene >> SOX13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204126103:204126103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1838G>T
AA Mutation	p.Ser613Ile(p.S613I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204116617:204116617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Ala177Thr(p.A177T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204124838:204124838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573C>T
AA Mutation	p.Arg525Cys(p.R525C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204114388:204114388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>T
AA Mutation	p.Ser96Phe(p.S96F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204116621:204116621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377320241
CDS Mutation	c.533C>T
AA Mutation	p.Ala178Val(p.A178V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204125976:204125976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1711A>G
AA Mutation	p.Met571Val(p.M571V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204124728:204124728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1463A>G
AA Mutation	p.Tyr488Cys(p.Y488C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367204
Start	204125924:204125924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370195383
CDS Mutation	c.1659G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367204
Start	204122903:204122903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367204
Start	204116640:204116640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367204
Start	204122338:204122338(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.969delC
AA Mutation	p.Ser324AlafsTer82(p.S324Afs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367204
Start	204122356:204122356(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.984delC
AA Mutation	p.Thr329ArgfsTer77(p.T329Rfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367204
Start	204122380:204122380(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1010delC
AA Mutation	p.Pro337ArgfsTer69(p.P337Rfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367204
Start	204122337:204122338(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs774299220
CDS Mutation	c.969dupC
AA Mutation	p.Ser324GlnfsTer23(p.S324Qfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SOX13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204124700:204124700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Trp(p.R479W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367204
Start	204122923:204122923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094G>A
AA Mutation	p.Ser365Asn(p.S365N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367204
Start	204126077:204126077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200693347
CDS Mutation	c.1812C>T
Mutation Classification	Silent
Feature Type	Transcript