Colon Cancer: Gene >> TNFAIP2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000333007
Start	103133515:103133515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745552776
CDS Mutation	c.1699C>T
AA Mutation	p.His567Tyr(p.H567Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103130029:103130029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>T
AA Mutation	p.Ala335Ser(p.A335S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103135310:103135310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1915G>A
AA Mutation	p.Gly639Arg(p.G639R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103126593:103126593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>A
AA Mutation	p.Val46Ile(p.V46I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103135314:103135314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202066956
CDS Mutation	c.1919C>T
AA Mutation	p.Ala640Val(p.A640V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103126576:103126576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119T>C
AA Mutation	p.Leu40Pro(p.L40P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103126675:103126675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218A>T
AA Mutation	p.Asp73Val(p.D73V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103132784:103132784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533232691
CDS Mutation	c.1457C>T
AA Mutation	p.Ala486Val(p.A486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103126554:103126554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97A>G
AA Mutation	p.Lys33Glu(p.K33E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333007
Start	103127585:103127585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333007
Start	103126670:103126670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFAIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333007
Start	103131062:103131062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781694049
CDS Mutation	c.1210G>A
AA Mutation	p.Ala404Thr(p.A404T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000333007
Start	103130393:103130393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Glu393Ter(p.E393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript