Colon Cancer: Gene >> ADAM19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157497059:157497059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429C>G
AA Mutation	p.Gln477Glu(p.Q477E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157505732:157505732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067A>C
AA Mutation	p.Asp356Ala(p.D356A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157489106:157489106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2321G>A
AA Mutation	p.Arg774Gln(p.R774Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157488351:157488351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536485712
CDS Mutation	c.2464G>A
AA Mutation	p.Gly822Arg(p.G822R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157518834:157518834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Asp219Asn(p.D219N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157519933:157519933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752116586
CDS Mutation	c.506C>T
AA Mutation	p.Pro169Leu(p.P169L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157509347:157509347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Cys(p.R287C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157488273:157488273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146122567
CDS Mutation	c.2542G>A
AA Mutation	p.Val848Ile(p.V848I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157493167:157493167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714T>C
AA Mutation	p.Cys572Arg(p.C572R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157490389:157490389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161T>C
AA Mutation	p.Tyr721His(p.Y721H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157509314:157509314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>A
AA Mutation	p.Ala298Thr(p.A298T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157481835:157481835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2659G>A
AA Mutation	p.Ala887Thr(p.A887T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517905
Start	157505764:157505764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143031163
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517905
Start	157481923:157481923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758375371
CDS Mutation	c.2571G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517905
Start	157537940:157537940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517905
Start	157481902:157481902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2592A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000517905
Start	157481735:157481735(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2759delG
AA Mutation	p.Gly920AlafsTer47(p.G920Afs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000517905
Start	157488434:157488434(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2381delC
AA Mutation	p.Pro794LeufsTer18(p.P794Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517905
Start	157488476:157488476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755386906
CDS Mutation	c.2339C>T
AA Mutation	p.Pro780Leu(p.P780L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000517905
Start	157488288:157488289(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs769171707
CDS Mutation	c.2526dupC
AA Mutation	p.Ala843ArgfsTer81(p.A843Rfs*81)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript