Colon Cancer: Gene >> ZNRF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29049481:29049481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779844636
CDS Mutation	c.1300G>A
AA Mutation	p.Gly434Ser(p.G434S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29050112:29050112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1931G>A
AA Mutation	p.Gly644Asp(p.G644D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29049382:29049382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Trp(p.R401W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29043333:29043333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>T
AA Mutation	p.Pro179Leu(p.P179L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29043420:29043420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368142754
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29046792:29046792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770632315
CDS Mutation	c.821G>A
AA Mutation	p.Arg274His(p.R274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000544604
Start	29043360:29043360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>T
AA Mutation	p.Ala188Val(p.A188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000544604
Start	29048433:29048433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752839337
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000544604
Start	28987183:28987183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000544604
Start	28987105:28987105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000544604
Start	29049220:29049221(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1046_1047delTG
AA Mutation	p.Val349GlyfsTer117(p.V349Gfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000544604
Start	29049655:29049655(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1477delC
AA Mutation	p.Arg493GlyfsTer77(p.R493Gfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000544604
Start	29050549:29050549(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2372delG
AA Mutation	p.Gly791AlafsTer14(p.G791Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000544604
Start	29044808:29044808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.665delT
AA Mutation	p.Phe222SerfsTer21(p.F222Sfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000544604
Start	29046809:29046809(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.841delG
AA Mutation	p.Ala281ProfsTer58(p.A281Pfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000544604
Start	29050623:29050623(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2442delA
AA Mutation	p.Pro815ArgfsTer11(p.P815Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000544604
Start	29050756:29050756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575C>T
AA Mutation	p.Arg859Ter(p.R859*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000544604
Start	29044879:29044879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Ter(p.R245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000544604
Start	29048475:29048475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999T>A
AA Mutation	p.Cys333Ter(p.C333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000544604
Start	29043401:29043401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Ter(p.R202*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNRF3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000544604
Start	28987192:28987192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417C>G
Mutation Classification	Silent
Feature Type	Transcript