Colon Cancer: Gene >> CDYL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80633230:80633230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770332841
CDS Mutation	c.623C>A
AA Mutation	p.Ala208Asp(p.A208D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80684744:80684744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410A>G
AA Mutation	p.Tyr137Cys(p.Y137C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80612678:80612678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768656038
CDS Mutation	c.1166C>T
AA Mutation	p.Thr389Met(p.T389M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80612685:80612685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159C>T
AA Mutation	p.Arg387Cys(p.R387C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80620781:80620781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80633071:80633071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778603352
CDS Mutation	c.782C>T
AA Mutation	p.Thr261Met(p.T261M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80612715:80612715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>A
AA Mutation	p.Ala377Thr(p.A377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80612666:80612666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178G>C
AA Mutation	p.Cys393Ser(p.C393S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80633110:80633110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>A
AA Mutation	p.Arg248Gln(p.R248Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80684549:80684549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605A>G
AA Mutation	p.Glu202Gly(p.E202G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000570137
Start	80620867:80620867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141862110
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000570137
Start	80620891:80620891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767400567
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000570137
Start	80685040:80685040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000570137
Start	80684800:80684800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.354delA
AA Mutation	p.Tyr120IlefsTer27(p.Y120Ifs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDYL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80620902:80620902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>A
AA Mutation	p.Ala290Thr(p.A290T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80684919:80684919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
AA Mutation	p.Arg79Cys(p.R79C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80684659:80684659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495G>T
AA Mutation	p.Lys165Asn(p.K165N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80604465:80604465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444C>T
AA Mutation	p.Leu482Phe(p.L482F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000570137
Start	80685097:80685097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57G>T
AA Mutation	p.Lys19Asn(p.K19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript