Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TWF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43797381:43797381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>T
AA Mutation	p.Lys227Asn(p.K227N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43797013:43797013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845T>G
AA Mutation	p.Ile282Ser(p.I282S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43799450:43799450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431C>A
AA Mutation	p.Pro144His(p.P144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43800512:43800512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301T>C
AA Mutation	p.Tyr101His(p.Y101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395510
Start	43800513:43800513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395510
Start	43797436:43797436(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.626delA
AA Mutation	p.Asn209MetfsTer4(p.N209Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TWF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43796991:43796991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867G>T
AA Mutation	p.Met289Ile(p.M289I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43799476:43799476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405A>C
AA Mutation	p.Lys135Asn(p.K135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395510
Start	43802323:43802323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245A>C
AA Mutation	p.Glu82Ala(p.E82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395510
Start	43795654:43795654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755933337
CDS Mutation	c.984T>C
Mutation Classification	Silent
Feature Type	Transcript