Colon Cancer: Gene >> RYK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134159260:134159260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1698G>T
AA Mutation	p.Gln566His(p.Q566H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134211568:134211568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394G>A
AA Mutation	p.Ala132Thr(p.A132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134188865:134188865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083A>C
AA Mutation	p.Glu361Asp(p.E361D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134222441:134222441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331T>G
AA Mutation	p.Phe111Val(p.F111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134188884:134188884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064A>G
AA Mutation	p.Glu355Gly(p.E355G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134188917:134188917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1031T>A
AA Mutation	p.Phe344Tyr(p.F344Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134175665:134175665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144378986
CDS Mutation	c.1528C>T
AA Mutation	p.Arg510Cys(p.R510C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134178057:134178057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198A>G
AA Mutation	p.Thr400Ala(p.T400A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134188915:134188915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033G>T
AA Mutation	p.Gly345Trp(p.G345W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620660
Start	134159320:134159320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373422007
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620660
Start	134222427:134222427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762957307
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620660
Start	134209822:134209822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000620660
Start	134209739:134209739(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.545delA
AA Mutation	p.Asn182IlefsTer5(p.N182Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000620660
Start	134209702:134209702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.582C>A
AA Mutation	p.Cys194Ter(p.C194*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RYK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134191960:134191960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Trp(p.R305W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134159270:134159270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748716502
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563Gln(p.R563Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000620660
Start	134175990:134175990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364G>T
AA Mutation	p.Gly455Val(p.G455V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript