Colon Cancer: Gene >> TGM3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381458
Start	2332004:2332004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336T>G
AA Mutation	p.Ser446Ala(p.S446A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2310312:2310312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146616453
CDS Mutation	c.316G>A
AA Mutation	p.Ala106Thr(p.A106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2340567:2340567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767808303
CDS Mutation	c.2068G>A
AA Mutation	p.Asp690Asn(p.D690N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2309724:2309724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75C>A
AA Mutation	p.Phe25Leu(p.F25L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2335122:2335122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649A>C
AA Mutation	p.Glu550Ala(p.E550A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381458
Start	2339986:2339986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933G>A
AA Mutation	p.Asp645Asn(p.D645N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2328140:2328140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375988138
CDS Mutation	c.1108G>A
AA Mutation	p.Ala370Thr(p.A370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2310253:2310253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774924175
CDS Mutation	c.257C>T
AA Mutation	p.Ala86Val(p.A86V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2332113:2332113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445G>A
AA Mutation	p.Ser482Asn(p.S482N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2317204:2317204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150052126
CDS Mutation	c.806G>A
AA Mutation	p.Arg269Gln(p.R269Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381458
Start	2340435:2340435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760313314
CDS Mutation	c.1936G>A
AA Mutation	p.Val646Met(p.V646M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2340471:2340471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760403495
CDS Mutation	c.1972C>T
AA Mutation	p.Arg658Cys(p.R658C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381458
Start	2332075:2332075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367986861
CDS Mutation	c.1407G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381458
Start	2328133:2328133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000381458
Start	2311127:2311127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>T
AA Mutation	p.Gln180Ter(p.Q180*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000381458
Start	2328158:2328158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754241815
CDS Mutation	c.1126C>T
AA Mutation	p.Arg376Ter(p.R376*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TGM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381458
Start	2309807:2309807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158G>T
AA Mutation	p.Arg53Ile(p.R53I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381458
Start	2312915:2312915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript