Colon Cancer: Gene >> MAGEC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141895533:141895533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760095164
CDS Mutation	c.1097C>T
AA Mutation	p.Ala366Val(p.A366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897014:141897014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256G>A
AA Mutation	p.Cys419Tyr(p.C419Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141865513:141865513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166C>T
AA Mutation	p.Leu56Phe(p.L56F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897683:141897683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1783A>G
AA Mutation	p.Ile595Val(p.I595V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897731:141897731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831A>G
AA Mutation	p.Met611Val(p.M611V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141879320:141879320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404G>T
AA Mutation	p.Arg135Ile(p.R135I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881696:141881696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809T>C
AA Mutation	p.Met270Thr(p.M270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881615:141881615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728A>G
AA Mutation	p.Glu243Gly(p.E243G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897007:141897007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249G>T
AA Mutation	p.Asp417Tyr(p.D417Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141895309:141895309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950G>A
AA Mutation	p.Arg317Gln(p.R317Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881789:141881789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>T
AA Mutation	p.Ala301Val(p.A301V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881471:141881471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584T>G
AA Mutation	p.Leu195Arg(p.L195R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881428:141881428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541A>T
AA Mutation	p.Thr181Ser(p.T181S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881407:141881407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.Pro174Ser(p.P174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141865489:141865489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>T
AA Mutation	p.Asp48Tyr(p.D48Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897813:141897813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1913C>T
AA Mutation	p.Thr638Ile(p.T638I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897425:141897425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667T>A
AA Mutation	p.Ile556Asn(p.I556N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897476:141897476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718G>C
AA Mutation	p.Ser573Thr(p.S573T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141897210:141897210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141881694:141881694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141896964:141896964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141879240:141879240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182076629
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141881667:141881667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141879390:141879390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373457144
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141897655:141897655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775063731
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298296
Start	141865477:141865477(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.134delA
AA Mutation	p.Lys45ArgfsTer15(p.K45Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298296
Start	141879413:141879413(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.502delG
AA Mutation	p.Glu168ArgfsTer45(p.E168Rfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000298296
Start	141897274:141897274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516G>T
AA Mutation	p.Glu506Ter(p.E506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897779:141897779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879G>T
AA Mutation	p.Ala627Ser(p.A627S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141881526:141881526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639T>G
AA Mutation	p.Asn213Lys(p.N213K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141896900:141896900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298296
Start	141897415:141897415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1657C>A
AA Mutation	p.Leu553Ile(p.L553I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298296
Start	141897240:141897240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000298296
Start	141897650:141897650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750G>T
AA Mutation	p.Glu584Ter(p.E584*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript