Colon Cancer: Gene >> RTN4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000337526
Start	55027484:55027484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615A>C
AA Mutation	p.Glu205Asp(p.E205D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55025306:55025306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2793A>C
AA Mutation	p.Lys931Asn(p.K931N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55026271:55026271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828G>A
AA Mutation	p.Val610Ile(p.V610I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	54973829:54973829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777282392
CDS Mutation	c.3469C>T
AA Mutation	p.Arg1157Trp(p.R1157W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	54987561:54987561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3151A>G
AA Mutation	p.Thr1051Ala(p.T1051A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55026843:55026843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256A>C
AA Mutation	p.Lys419Thr(p.K419T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55026961:55026961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749220120
CDS Mutation	c.1138A>G
AA Mutation	p.Met380Val(p.M380V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55025730:55025730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779152319
CDS Mutation	c.2369C>T
AA Mutation	p.Ala790Val(p.A790V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55025297:55025297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2802C>A
AA Mutation	p.Phe934Leu(p.F934L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55025538:55025538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2561G>T
AA Mutation	p.Arg854Ile(p.R854I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337526
Start	55026395:55026395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337526
Start	55025417:55025417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2682A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337526
Start	55026092:55026092(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2007delA
AA Mutation	p.Val670TyrfsTer4(p.V670Yfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337526
Start	55026830:55026830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1269delA
AA Mutation	p.Lys423AsnfsTer32(p.K423Nfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000337526
Start	55025989:55025989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2110G>T
AA Mutation	p.Glu704Ter(p.E704*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000337526
Start	54987678:54987678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3034A>T
AA Mutation	p.Arg1012Ter(p.R1012*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000337526
Start	54973161:54973161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3574G>T
AA Mutation	p.Glu1192Ter(p.E1192*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000337526
Start	55027357:55027357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>T
AA Mutation	p.Glu248Ter(p.E248*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337526
Start	55027080:55027081(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1018dupC
AA Mutation	p.Leu340ProfsTer3(p.L340Pfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337526
Start	55026091:55026092(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2007dupA
AA Mutation	p.Val670SerfsTer9(p.V670Sfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337526
Start	55025195:55025196(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2903_2904insGGAATGTTCCC
AA Mutation	p.Lys969GlufsTer10(p.K969Efs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337526
Start	55025537:55025538(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2561_2562insTT
AA Mutation	p.Arg854SerfsTer2(p.R854Sfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RTN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55025621:55025621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2478G>T
AA Mutation	p.Glu826Asp(p.E826D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55025699:55025699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2400G>T
AA Mutation	p.Leu800Phe(p.L800F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55027365:55027365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.734C>A
AA Mutation	p.Ser245Tyr(p.S245Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337526
Start	55027045:55027045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054A>C
AA Mutation	p.Lys352Gln(p.K352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript