Colon Cancer: Gene >> TGM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260448:43260448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Trp(p.R48W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43234861:43234861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777999621
CDS Mutation	c.1783C>T
AA Mutation	p.Arg595Cys(p.R595C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260502:43260502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>T
AA Mutation	p.His30Tyr(p.H30Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43238846:43238846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754853779
CDS Mutation	c.1316A>G
AA Mutation	p.Asp439Gly(p.D439G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43256591:43256591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532C>A
AA Mutation	p.Pro178Thr(p.P178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43234860:43234860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145147059
CDS Mutation	c.1784G>A
AA Mutation	p.Arg595His(p.R595H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260156:43260156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759563503
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260157:43260157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768591773
CDS Mutation	c.331G>T
AA Mutation	p.Ala111Ser(p.A111S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43252822:43252822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761166440
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43252773:43252773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848C>T
AA Mutation	p.Ala283Val(p.A283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260486:43260486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749224503
CDS Mutation	c.104G>A
AA Mutation	p.Arg35Gln(p.R35Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220420
Start	43260400:43260400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190G>A
AA Mutation	p.Gly64Arg(p.G64R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43252771:43252771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144575810
CDS Mutation	c.850G>A
AA Mutation	p.Val284Ile(p.V284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43238897:43238897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265C>A
AA Mutation	p.Ser422Tyr(p.S422Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43235771:43235771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412G>T
AA Mutation	p.Gly471Val(p.G471V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220420
Start	43238857:43238857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746187832
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220420
Start	43238854:43238854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220420
Start	43252847:43252847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751456953
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220420
Start	43235710:43235710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220420
Start	43233203:43233203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2151C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TGM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43235709:43235709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763381962
CDS Mutation	c.1474C>T
AA Mutation	p.Arg492Trp(p.R492W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43240987:43240987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866T>G
AA Mutation	p.Met289Arg(p.M289R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43235567:43235567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1616T>C
AA Mutation	p.Leu539Pro(p.L539P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43238836:43238836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1326G>T
AA Mutation	p.Glu442Asp(p.E442D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260124:43260124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>A
AA Mutation	p.Asp122Asn(p.D122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43235622:43235622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561C>G
AA Mutation	p.Gln521Glu(p.Q521E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43233606:43233606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957T>G
AA Mutation	p.Cys653Gly(p.C653G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43240903:43240903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765336664
CDS Mutation	c.950A>G
AA Mutation	p.Tyr317Cys(p.Y317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000220420
Start	43260102:43260102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386C>T
AA Mutation	p.Thr129Met(p.T129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript