Colon Cancer: Gene >> RTKN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62199850:62199850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.His400Tyr(p.H400Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62218247:62218247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836C>T
AA Mutation	p.Ala279Val(p.A279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62198116:62198116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622T>C
AA Mutation	p.Leu541Ser(p.L541S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62236206:62236206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546A>C
AA Mutation	p.Glu182Asp(p.E182D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62241189:62241189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758667603
CDS Mutation	c.323G>A
AA Mutation	p.Arg108Gln(p.R108Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62197950:62197950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788A>C
AA Mutation	p.Lys596Asn(p.K596N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62262674:62262674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208T>A
AA Mutation	p.Ser70Thr(p.S70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62198315:62198315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423G>C
AA Mutation	p.Asp475His(p.D475H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373789
Start	62198390:62198390(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs765032947
CDS Mutation	c.1348delA
AA Mutation	p.Ile450LeufsTer67(p.I450Lfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000373789
Start	62241142:62241142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756858537
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Ter(p.R124*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000373789
Start	62262785:62262785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772033296
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Ter(p.R33*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RTKN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373789
Start	62246016:62246016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>T
AA Mutation	p.Gly100Val(p.G100V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373789
Start	62204969:62204969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000373789
Start	62262785:62262785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772033296
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Ter(p.R33*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript