Colon Cancer: Gene >> ADAM9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39077386:39077386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1856A>G
AA Mutation	p.Glu619Gly(p.E619G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39017299:39017299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760058275
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39090137:39090137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2159G>T
AA Mutation	p.Arg720Met(p.R720M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39077317:39077317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138482520
CDS Mutation	c.1787G>A
AA Mutation	p.Arg596Gln(p.R596Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39018905:39018905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659T>C
AA Mutation	p.Val220Ala(p.V220A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39021651:39021651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>A
AA Mutation	p.Met227Ile(p.M227I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39055602:39055602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421G>A
AA Mutation	p.Arg474Gln(p.R474Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39077270:39077270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1740G>T
AA Mutation	p.Glu580Asp(p.E580D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39090070:39090070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770679072
CDS Mutation	c.2092G>A
AA Mutation	p.Gly698Arg(p.G698R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000487273
Start	39041967:39041967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1152T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000487273
Start	39103691:39103691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2451C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000487273
Start	38997112:38997112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780389156
CDS Mutation	c.49T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000487273
Start	39011682:39011682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>T
AA Mutation	p.Gly74Ter(p.G74*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000487273
Start	39023257:39023258(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.847_848insGAAAGAAATAAA
AA Mutation	p.Gly282_Asn283insArgLysLysTer(p.G282_N283insRKK*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000487273
Start	39083037:39083038(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2032_2033insGGAAACC
AA Mutation	p.Tyr678TrpfsTer15(p.Y678Wfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39017299:39017299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760058275
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39090164:39090164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2186G>T
AA Mutation	p.Arg729Ile(p.R729I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39026788:39026788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108T>C
AA Mutation	p.Cys370Arg(p.C370R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39007952:39007952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>T
AA Mutation	p.Arg55Ile(p.R55I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000487273
Start	39077323:39077323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793C>G
AA Mutation	p.Thr598Ser(p.T598S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000487273
Start	39091341:39091341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2293G>T
AA Mutation	p.Glu765Ter(p.E765*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript