Colon Cancer: Gene >> ELF3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359651
Start	202011299:202011299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163G>A
AA Mutation	p.Glu55Lys(p.E55K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359651
Start	202012679:202012679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Gly173Asp(p.G173D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359651
Start	202012398:202012398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.440G>T
AA Mutation	p.Gly147Val(p.G147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359651
Start	202013020:202013020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778952302
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202011224:202011224(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.92delC
AA Mutation	p.Pro31LeufsTer12(p.P31Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202015230:202015230(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1024delC
AA Mutation	p.Leu342TrpfsTer105(p.L342Wfs*105)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202013938:202013938(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.916delC
AA Mutation	p.Leu306CysfsTer19(p.L306Cfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000359651
Start	202013968:202013968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945G>A
AA Mutation	p.Trp315Ter(p.W315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202011990:202011991(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.198dupC
AA Mutation	p.Trp67LeufsTer25(p.W67Lfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202012723:202012724(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.567dupC
AA Mutation	p.Ser190LeufsTer6(p.S190Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000359651
Start	202013035:202013036(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.688+1dupG
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant;coding_sequence_variant
Transcription ID	ENST00000359651
Start	202013288:202013300(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.799_805+6delAAGCACGGTGAGC
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ELF3

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202013938:202013938(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.916delC
AA Mutation	p.Leu306CysfsTer19(p.L306Cfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000359651
Start	202013277:202013277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>T
AA Mutation	p.Glu262Ter(p.E262*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359651
Start	202012645:202012646(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.485_486dupGC
AA Mutation	p.Ser163AlafsTer92(p.S163Afs*92)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript