Colon Cancer: Gene >> MET

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116769745:116769745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199502137
CDS Mutation	c.2684C>T
AA Mutation	p.Thr895Met(p.T895M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116699692:116699692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608C>A
AA Mutation	p.Ser203Tyr(p.S203Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116757474:116757474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1900T>C
AA Mutation	p.Phe634Leu(p.F634L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116775001:116775001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3149C>T
AA Mutation	p.Thr1050Ile(p.T1050I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116777425:116777425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780431412
CDS Mutation	c.3296A>G
AA Mutation	p.Asp1099Gly(p.D1099G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116731746:116731746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376364468
CDS Mutation	c.1279G>A
AA Mutation	p.Val427Ile(p.V427I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116757660:116757660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376459715
CDS Mutation	c.1988C>T
AA Mutation	p.Ser663Leu(p.S663L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116699596:116699596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512A>G
AA Mutation	p.Gln171Arg(p.Q171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116759453:116759453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327T>A
AA Mutation	p.Val776Asp(p.V776D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116795907:116795907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3956G>A
AA Mutation	p.Cys1319Tyr(p.C1319Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116731803:116731803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779022887
CDS Mutation	c.1336A>G
AA Mutation	p.Ile446Val(p.I446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116763120:116763120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435A>G
AA Mutation	p.Gln812Arg(p.Q812R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116700124:116700124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1040C>T
AA Mutation	p.Ala347Val(p.A347V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116699121:116699121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>C
AA Mutation	p.Val13Leu(p.V13L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116731701:116731701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234C>A
AA Mutation	p.Arg412Ser(p.R412S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397752
Start	116757774:116757774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2102G>T
AA Mutation	p.Ser701Ile(p.S701I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116740856:116740856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371124109
CDS Mutation	c.1532C>T
AA Mutation	p.Thr511Met(p.T511M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116699767:116699767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683T>G
AA Mutation	p.Phe228Cys(p.F228C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000397752
Start	116755374:116755374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1721C>G
AA Mutation	p.Pro574Arg(p.P574R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116763184:116763184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2499C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116699720:116699720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.636T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116771596:116771596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2829A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116699489:116699489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200494620
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116700152:116700152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116795765:116795765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3909A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397752
Start	116795965:116795965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4014A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000397752
Start	116778943:116778943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3508C>T
AA Mutation	p.Arg1170Ter(p.R1170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MET

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000397752
Start	116763237:116763237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2552C>A
AA Mutation	p.Ser851Ter(p.S851*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000397752
Start	116778943:116778943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3508C>T
AA Mutation	p.Arg1170Ter(p.R1170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript