Colon Cancer: Gene >> TGM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24259131:24259131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199786703
CDS Mutation	c.1103C>T
AA Mutation	p.Thr368Met(p.T368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24249449:24249449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2318C>T
AA Mutation	p.Pro773Leu(p.P773L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24254156:24254156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141864003
CDS Mutation	c.2221G>A
AA Mutation	p.Val741Ile(p.V741I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24262288:24262288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201774398
CDS Mutation	c.65C>T
AA Mutation	p.Thr22Met(p.T22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24259769:24259769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121918731
CDS Mutation	c.919C>T
AA Mutation	p.Arg307Trp(p.R307W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24255166:24255166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733A>G
AA Mutation	p.Asp578Gly(p.D578G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24262253:24262253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149148326
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Cys(p.R34C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24254215:24254215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2162T>G
AA Mutation	p.Leu721Arg(p.L721R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000206765
Start	24260638:24260638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>C
AA Mutation	p.Ser190Thr(p.S190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206765
Start	24262158:24262158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000206765
Start	24254825:24254825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1928-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TGM1

No Mutation Annotation!