Colon Cancer: Gene >> SOX21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376945
Start	94711991:94711991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59G>A
AA Mutation	p.Arg20Gln(p.R20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376945
Start	94711884:94711884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166C>T
AA Mutation	p.Pro56Ser(p.P56S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376945
Start	94711980:94711980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Cys(p.R24C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376945
Start	94711992:94711992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>T
AA Mutation	p.Arg20Trp(p.R20W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376945
Start	94711863:94711863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Cys(p.R63C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376945
Start	94711921:94711921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376945
Start	94711960:94711960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376945
Start	94711990:94711990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SOX21

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376945
Start	94711798:94711798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765306743
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript