Colon Cancer: Gene >> WIPF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323571
Start	40273817:40273817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323571
Start	40264585:40264585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409G>A
AA Mutation	p.Asp137Asn(p.D137N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323571
Start	40262566:40262566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238G>T
AA Mutation	p.Ala80Ser(p.A80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323571
Start	40277122:40277122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220A>G
AA Mutation	p.Asp407Gly(p.D407G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323571
Start	40264638:40264638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323571
Start	40264845:40264845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323571
Start	40273930:40273930(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1115delC
AA Mutation	p.Pro372LeufsTer7(p.P372Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323571
Start	40256484:40256484(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.29delC
AA Mutation	p.Pro10HisfsTer20(p.P10Hfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323571
Start	40264789:40264792(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.616_619delGAGA
AA Mutation	p.Glu206AsnfsTer31(p.E206Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WIPF2

No Mutation Annotation!