Colon Cancer: Gene >> IGDCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65386031:65386031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2980G>A
AA Mutation	p.Ala994Thr(p.A994T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65395199:65395199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749510394
CDS Mutation	c.1471C>T
AA Mutation	p.Arg491Trp(p.R491W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65389386:65389386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368140698
CDS Mutation	c.2434G>A
AA Mutation	p.Gly812Ser(p.G812S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65395118:65395118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552G>A
AA Mutation	p.Ala518Thr(p.A518T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65392223:65392223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2033G>A
AA Mutation	p.Arg678His(p.R678H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65394441:65394441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684T>C
AA Mutation	p.Tyr562His(p.Y562H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65385013:65385013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3283C>T
AA Mutation	p.Pro1095Ser(p.P1095S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65396927:65396927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65390290:65390290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758067780
CDS Mutation	c.2273C>T
AA Mutation	p.Ala758Val(p.A758V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65389317:65389317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202013326
CDS Mutation	c.2503G>A
AA Mutation	p.Gly835Ser(p.G835S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65388813:65388813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200877185
CDS Mutation	c.2702C>T
AA Mutation	p.Thr901Met(p.T901M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352385
Start	65395886:65395886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352385
Start	65388902:65388902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2613delC
AA Mutation	p.Thr872GlnfsTer11(p.T872Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352385
Start	65385981:65385981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771839118
CDS Mutation	c.3030delC
AA Mutation	p.Ser1011AlafsTer59(p.S1011Afs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352385
Start	65388940:65388940(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2575delC
AA Mutation	p.Leu859Ter(p.L859*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352385
Start	65386022:65386023(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2988_2989insCG
AA Mutation	p.Gly997ArgfsTer74(p.G997Rfs*74)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IGDCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352385
Start	65395199:65395199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749510394
CDS Mutation	c.1471C>T
AA Mutation	p.Arg491Trp(p.R491W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352385
Start	65411276:65411276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352385
Start	65396892:65396892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758027877
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript