Colon Cancer: Gene >> SOX17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54459219:54459219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.His157Tyr(p.H157Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54458358:54458358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>A
AA Mutation	p.Ala74Thr(p.A74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54459829:54459829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54458338:54458338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200G>A
AA Mutation	p.Arg67His(p.R67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54459093:54459093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Trp(p.R115W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54459963:54459963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213G>A
AA Mutation	p.Ala405Thr(p.A405T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54459804:54459804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>T
AA Mutation	p.Ala352Ser(p.A352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297316
Start	54458405:54458405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297316
Start	54458351:54458351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297316
Start	54459857:54459857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201582946
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297316
Start	54459953:54459953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367836623
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297316
Start	54459749:54459749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SOX17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297316
Start	54459174:54459174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript