Colon Cancer: Gene >> ADAM28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24326627:24326627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139736903
CDS Mutation	c.964G>A
AA Mutation	p.Val322Ile(p.V322I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24332697:24332697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1319A>G
AA Mutation	p.Lys440Arg(p.K440R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24332666:24332666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762484740
CDS Mutation	c.1288A>G
AA Mutation	p.Thr430Ala(p.T430A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24320245:24320245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>T
AA Mutation	p.Asp196Tyr(p.D196Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24323919:24323919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806C>T
AA Mutation	p.Ala269Val(p.A269V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24335497:24335497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>T
AA Mutation	p.Pro475Ser(p.P475S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265769
Start	24335490:24335490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771905381
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265769
Start	24341637:24341637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145453785
CDS Mutation	c.1710G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265769
Start	24309953:24309953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265769
Start	24294167:24294167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265769
Start	24309960:24309960(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770638998
CDS Mutation	c.224delA
AA Mutation	p.Asn75ThrfsTer53(p.N75Tfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265769
Start	24309959:24309960(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.223_224dupAA
AA Mutation	p.Asn75LysfsTer54(p.N75Kfs*54)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265769
Start	24309959:24309960(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs570442888
CDS Mutation	c.224dupA
AA Mutation	p.Asn75LysfsTer15(p.N75Kfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265769
Start	24300079:24300079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24329994:24329994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982G>A
AA Mutation	p.Asp328Asn(p.D328N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24349918:24349918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2045T>C
AA Mutation	p.Val682Ala(p.V682A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24300031:24300031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104G>T
AA Mutation	p.Arg35Ile(p.R35I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24323935:24323935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>T
AA Mutation	p.Glu274Asp(p.E274D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24310236:24310236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301A>T
AA Mutation	p.Ile101Phe(p.I101F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265769
Start	24311404:24311404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350C>A
AA Mutation	p.Ser117Tyr(p.S117Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript