Colon Cancer: Gene >> TGM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44903901:44903901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768242363
CDS Mutation	c.989C>T
AA Mutation	p.Thr330Met(p.T330M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44901847:44901847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887A>G
AA Mutation	p.His296Arg(p.H296R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44911291:44911291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798G>C
AA Mutation	p.Gly600Arg(p.G600R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44911038:44911038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1687G>T
AA Mutation	p.Gly563Cys(p.G563C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44887740:44887740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754139975
CDS Mutation	c.245C>T
AA Mutation	p.Thr82Met(p.T82M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44901640:44901640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>A
AA Mutation	p.Asn258Lys(p.N258K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44911323:44911323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830G>T
AA Mutation	p.Lys610Asn(p.K610N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44911334:44911334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144767494
CDS Mutation	c.1841C>T
AA Mutation	p.Ala614Val(p.A614V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44885415:44885415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110G>A
AA Mutation	p.Arg37Gln(p.R37Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44903963:44903963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768311392
CDS Mutation	c.1051G>A
AA Mutation	p.Ala351Thr(p.A351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296125
Start	44885374:44885374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.69T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296125
Start	44911342:44911342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296125
Start	44890659:44890659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778730711
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000296125
Start	44885357:44885357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52C>T
AA Mutation	p.Gln18Ter(p.Q18*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296125
Start	44910324:44910325(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1566dupA
AA Mutation	p.Leu523ThrfsTer3(p.L523Tfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TGM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44901828:44901828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868A>G
AA Mutation	p.Thr290Ala(p.T290A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296125
Start	44903890:44903890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978C>A
AA Mutation	p.Phe326Leu(p.F326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296125
Start	44907025:44907025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138265891
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296125
Start	44890611:44890611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309G>C
Mutation Classification	Silent
Feature Type	Transcript