Colon Cancer: Gene >> DUSP22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	348191:348191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758237999
CDS Mutation	c.352G>A
AA Mutation	p.Val118Met(p.V118M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	311892:311892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147959810
CDS Mutation	c.68C>T
AA Mutation	p.Ala23Val(p.A23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	348125:348125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138056339
CDS Mutation	c.286G>A
AA Mutation	p.Val96Met(p.V96M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	345904:345904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140808686
CDS Mutation	c.239G>A
AA Mutation	p.Arg80His(p.R80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	348192:348192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353T>G
AA Mutation	p.Val118Gly(p.V118G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000344450
Start	350824:350824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>T
AA Mutation	p.Ala171Ser(p.A171S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	311906:311906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82A>G
AA Mutation	p.Lys28Glu(p.K28E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	348140:348140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768192099
CDS Mutation	c.301G>A
AA Mutation	p.Ala101Thr(p.A101T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	311891:311891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144879804
CDS Mutation	c.67G>A
AA Mutation	p.Ala23Thr(p.A23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344450
Start	348181:348181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344450
Start	348804:348804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000344450
Start	311894:311894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70G>T
AA Mutation	p.Glu24Ter(p.E24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	311937:311937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747637554
CDS Mutation	c.113A>G
AA Mutation	p.His38Arg(p.H38R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	304647:304647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41T>G
AA Mutation	p.Ile14Ser(p.I14S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344450
Start	350861:350861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548G>T
AA Mutation	p.Arg183Ile(p.R183I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344450
Start	345890:345890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369153482
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript