Colon Cancer: Gene >> ADAM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133270428:133270428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759368536
CDS Mutation	c.1717G>A
AA Mutation	p.Ala573Thr(p.A573T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133272830:133272830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Trp(p.R225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133268763:133268763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2048G>A
AA Mutation	p.Ser683Asn(p.S683N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133271021:133271021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1424T>C
AA Mutation	p.Leu475Pro(p.L475P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133271857:133271857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776195089
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352His(p.R352H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133271623:133271623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539019756
CDS Mutation	c.1189G>A
AA Mutation	p.Ala397Thr(p.A397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133271538:133271538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274G>C
AA Mutation	p.Gly425Ala(p.G425A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133268808:133268808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2003T>C
AA Mutation	p.Val668Ala(p.V668A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133274015:133274015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242C>T
AA Mutation	p.Ser81Phe(p.S81F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133270418:133270418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1727C>T
AA Mutation	p.Thr576Ile(p.T576I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133270886:133270886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1559G>A
AA Mutation	p.Gly520Glu(p.G520E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133263229:133263229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2402C>T
AA Mutation	p.Ala801Val(p.A801V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000445355
Start	133269513:133269513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1880A>C
AA Mutation	p.Gln627Pro(p.Q627P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445355
Start	133273371:133273371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775423816
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445355
Start	133271931:133271931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745919124
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445355
Start	133270426:133270426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770651639
CDS Mutation	c.1719G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445355
Start	133270943:133270943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1502delG
AA Mutation	p.Gly501AlafsTer144(p.G501Afs*144)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445355
Start	133271531:133271531(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1281delC
AA Mutation	p.Glu428ArgfsTer32(p.E428Rfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445355
Start	133273329:133273329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498C>A
Mutation Classification	Silent
Feature Type	Transcript