Colon Cancer: Gene >> DDR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162770441:162770441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773598662
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478His(p.R478H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162772144:162772144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1625C>T
AA Mutation	p.Ala542Val(p.A542V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162754815:162754815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756942296
CDS Mutation	c.377G>A
AA Mutation	p.Gly126Asp(p.G126D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162772140:162772140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621C>T
AA Mutation	p.Pro541Ser(p.P541S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162772154:162772154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635G>T
AA Mutation	p.Met545Ile(p.M545I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162754686:162754686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248T>G
AA Mutation	p.Leu83Arg(p.L83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162759953:162759953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829C>T
AA Mutation	p.Arg277Cys(p.R277C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162753161:162753161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149G>A
AA Mutation	p.Ser50Asn(p.S50N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162754841:162754841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371333028
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Cys(p.R135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162775687:162775687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779963287
CDS Mutation	c.1892G>A
AA Mutation	p.Arg631Gln(p.R631Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162770437:162770437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1429C>A
AA Mutation	p.Leu477Ile(p.L477I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162754751:162754751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759709680
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162778713:162778713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201041695
CDS Mutation	c.2417G>A
AA Mutation	p.Arg806Gln(p.R806Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162780238:162780238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771898787
CDS Mutation	c.2560G>A
AA Mutation	p.Asp854Asn(p.D854N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162754693:162754693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255G>C
AA Mutation	p.Glu85Asp(p.E85D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162770382:162770382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162775727:162775727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1932T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162772070:162772070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162759844:162759844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141801107
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162778678:162778678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2382T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000367921
Start	162755699:162755699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601C>T
AA Mutation	p.Gln201Ter(p.Q201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DDR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162772173:162772173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654G>T
AA Mutation	p.Asp552Tyr(p.D552Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162780238:162780238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771898787
CDS Mutation	c.2560G>A
AA Mutation	p.Asp854Asn(p.D854N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367921
Start	162773588:162773588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848G>T
AA Mutation	p.Lys616Asn(p.K616N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162761249:162761249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162754828:162754828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367921
Start	162775700:162775700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1905A>G
Mutation Classification	Silent
Feature Type	Transcript