Colon Cancer: Gene >> WNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293549
Start	48980678:48980678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>T
AA Mutation	p.Ala205Ser(p.A205S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293549
Start	48981222:48981222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>A
AA Mutation	p.Cys232Tyr(p.C232Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293549
Start	48979658:48979658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295A>G
AA Mutation	p.Asn99Asp(p.N99D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293549
Start	48980478:48980478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413C>T
AA Mutation	p.Ser138Leu(p.S138L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293549
Start	48980565:48980565(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.506delG
AA Mutation	p.Gly169AlafsTer30(p.G169Afs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293549
Start	48980564:48980565(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs779969402
CDS Mutation	c.506dupG
AA Mutation	p.Cys170LeufsTer6(p.C170Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WNT1

No Mutation Annotation!