Colon Cancer: Gene >> TM4SF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305354
Start	149498832:149498832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512T>A
AA Mutation	p.Met171Lys(p.M171K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305354
Start	149475836:149475836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188249785
CDS Mutation	c.188C>T
AA Mutation	p.Ala63Val(p.A63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305354
Start	149498817:149498817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497T>C
AA Mutation	p.Val166Ala(p.V166A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305354
Start	149487633:149487633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305354
Start	149474931:149474931(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.60delT
AA Mutation	p.Phe20LeufsTer16(p.F20Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305354
Start	149474930:149474931(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs776266010
CDS Mutation	c.60dupT
AA Mutation	p.Gly21TrpfsTer5(p.G21Wfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	start_lost
Transcription ID	ENST00000305354
Start	149474878:149474878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TM4SF4

No Mutation Annotation!