Colon Cancer: Gene >> WISP1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000250160
Start	133227411:133227411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.805G>A
AA Mutation	p.Ala269Thr(p.A269T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250160
Start	133212943:133212943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149A>G
AA Mutation	p.Lys50Arg(p.K50R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250160
Start	133227487:133227487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>A
AA Mutation	p.Arg294His(p.R294H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250160
Start	133220713:133220713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140648348
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250160
Start	133212976:133212976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182G>A
AA Mutation	p.Arg61His(p.R61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250160
Start	133213062:133213062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>A
AA Mutation	p.Ala90Thr(p.A90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250160
Start	133212962:133212962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533662816
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250160
Start	133213031:133213031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752374588
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250160
Start	133227608:133227608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250160
Start	133220747:133220747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150221105
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250160
Start	133220714:133220714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.488delC
AA Mutation	p.Pro163ArgfsTer11(p.P163Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250160
Start	133225475:133225475(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.700delG
AA Mutation	p.Val234SerfsTer50(p.V234Sfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000250160
Start	133213143:133213143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349C>T
AA Mutation	p.Gln117Ter(p.Q117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WISP1

No Mutation Annotation!