Colon Cancer: Gene >> AGRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1043293:1043293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439C>T
AA Mutation	p.Ala480Val(p.A480V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1046646:1046646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377535426
CDS Mutation	c.3161C>T
AA Mutation	p.Ala1054Val(p.A1054V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1048926:1048926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4165C>A
AA Mutation	p.Arg1389Ser(p.R1389S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1046193:1046193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2839G>A
AA Mutation	p.Glu947Lys(p.E947K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1042010:1042010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201787384
CDS Mutation	c.1232G>A
AA Mutation	p.Arg411His(p.R411H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1046550:1046550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777916390
CDS Mutation	c.3065C>T
AA Mutation	p.Ser1022Leu(p.S1022L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1054486:1054486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5915C>T
AA Mutation	p.Ala1972Val(p.A1972V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1053794:1053794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142132521
CDS Mutation	c.5693G>A
AA Mutation	p.Arg1898His(p.R1898H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1049046:1049046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201346452
CDS Mutation	c.4285C>T
AA Mutation	p.Arg1429Cys(p.R1429C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1054497:1054497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781607506
CDS Mutation	c.5926G>A
AA Mutation	p.Gly1976Ser(p.G1976S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1053934:1053934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145079121
CDS Mutation	c.5833G>A
AA Mutation	p.Val1945Met(p.V1945M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1043440:1043440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752221979
CDS Mutation	c.1586C>T
AA Mutation	p.Ala529Val(p.A529V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1020267:1020267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95C>T
AA Mutation	p.Pro32Leu(p.P32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1044249:1044249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755903720
CDS Mutation	c.2140G>A
AA Mutation	p.Gly714Ser(p.G714S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1050014:1050014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753675816
CDS Mutation	c.4856G>A
AA Mutation	p.Arg1619His(p.R1619H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1047829:1047829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3685G>T
AA Mutation	p.Val1229Leu(p.V1229L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1041643:1041643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747332721
CDS Mutation	c.1118C>T
AA Mutation	p.Ser373Leu(p.S373L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379370
Start	1049568:1049568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373657385
CDS Mutation	c.4517C>T
AA Mutation	p.Ala1506Val(p.A1506V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1049288:1049288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4351C>T
AA Mutation	p.Pro1451Ser(p.P1451S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1049917:1049917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4759G>T
AA Mutation	p.Asp1587Tyr(p.D1587Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1049666:1049666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4615G>T
AA Mutation	p.Ala1539Ser(p.A1539S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379370
Start	1045785:1045785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776485359
CDS Mutation	c.2589G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379370
Start	1054520:1054520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748240272
CDS Mutation	c.5949G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379370
Start	1047391:1047391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3453G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379370
Start	1045189:1045189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2283G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379370
Start	1045399:1045399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2412C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379370
Start	1043899:1043899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1880delC
AA Mutation	p.Pro627ArgfsTer105(p.P627Rfs*105)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379370
Start	1046497:1046497(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3016delC
AA Mutation	p.Leu1006TrpfsTer34(p.L1006Wfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000379370
Start	1045487:1045487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2500C>T
AA Mutation	p.Arg834Ter(p.R834*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000379370
Start	1042123:1042123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345C>T
AA Mutation	p.Gln449Ter(p.Q449*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379370
Start	1051469:1051469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774881136
CDS Mutation	c.5387G>A
AA Mutation	p.Arg1796His(p.R1796H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379370
Start	1045258:1045258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2352G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379370
Start	1049601:1049601(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4554delG
AA Mutation	p.Cys1519AlafsTer130(p.C1519Afs*130)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379370
Start	1050832:1050833(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.5249_5252dupCCCC
AA Mutation	p.Val1752ProfsTer120(p.V1752Pfs*120)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript