Colon Cancer: Gene >> SOX10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37973844:37973844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052A>G
AA Mutation	p.Asp351Gly(p.D351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37973761:37973761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758445473
CDS Mutation	c.1135G>A
AA Mutation	p.Ala379Thr(p.A379T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37983469:37983469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Trp(p.R106W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37973878:37973878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549034055
CDS Mutation	c.1018G>A
AA Mutation	p.Val340Met(p.V340M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37973586:37973586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753998628
CDS Mutation	c.1310C>T
AA Mutation	p.Thr437Met(p.T437M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37973865:37973865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199657550
CDS Mutation	c.1031C>T
AA Mutation	p.Thr344Met(p.T344M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37974118:37974118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367743809
CDS Mutation	c.778G>A
AA Mutation	p.Gly260Arg(p.G260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37978112:37978112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452G>A
AA Mutation	p.Arg151His(p.R151H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37983417:37983417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368C>T
AA Mutation	p.Ala123Val(p.A123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37983430:37983430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Cys(p.R119C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37973628:37973628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268C>T
AA Mutation	p.Ser423Leu(p.S423L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360880
Start	37983431:37983431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360880
Start	37974161:37974161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762449567
CDS Mutation	c.735G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SOX10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37978035:37978035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Trp(p.R177W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360880
Start	37983603:37983603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182G>C
AA Mutation	p.Gly61Ala(p.G61A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript