Colon Cancer: Gene >> TFR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100630972:100630972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396Gln(p.R396Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100627620:100627620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1724C>T
AA Mutation	p.Thr575Met(p.T575M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100627442:100627442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817A>G
AA Mutation	p.Asn606Ser(p.N606S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100621018:100621018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2245C>T
AA Mutation	p.Arg749Trp(p.R749W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100632167:100632167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>A
AA Mutation	p.Gly294Glu(p.G294E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100627279:100627279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1980C>A
AA Mutation	p.Phe660Leu(p.F660L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100633518:100633518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512G>A
AA Mutation	p.Gly171Glu(p.G171E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100628082:100628082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200053955
CDS Mutation	c.1528G>A
AA Mutation	p.Ala510Thr(p.A510T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223051
Start	100633031:100633031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223051
Start	100628248:100628248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41295899
CDS Mutation	c.1449C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223051
Start	100627625:100627625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223051
Start	100626789:100626790(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2109dupA
AA Mutation	p.Arg704ThrfsTer88(p.R704Tfs*88)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223051
Start	100631939:100631940(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.972_973insTGGG
AA Mutation	p.Leu325TrpfsTer119(p.L325Wfs*119)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TFR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100621074:100621074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779069147
CDS Mutation	c.2189G>A
AA Mutation	p.Arg730His(p.R730H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100641132:100641132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>C
AA Mutation	p.Gly44Arg(p.G44R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100627272:100627272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987G>A
AA Mutation	p.Asp663Asn(p.D663N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223051
Start	100627627:100627627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1717T>C
AA Mutation	p.Ser573Pro(p.S573P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript