Colon Cancer: Gene >> ZNF606

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57979838:57979838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842G>T
AA Mutation	p.Arg281Ile(p.R281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978434:57978434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2246C>A
AA Mutation	p.Ser749Tyr(p.S749Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57979186:57979186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494T>A
AA Mutation	p.His498Gln(p.H498Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978506:57978506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2174T>C
AA Mutation	p.Val725Ala(p.V725A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57988243:57988243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364T>G
AA Mutation	p.Ser122Ala(p.S122A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978917:57978917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1763G>T
AA Mutation	p.Arg588Ile(p.R588I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57979146:57979146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1534T>C
AA Mutation	p.Phe512Leu(p.F512L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978308:57978308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2372T>C
AA Mutation	p.Leu791Pro(p.L791P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57979046:57979046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634G>A
AA Mutation	p.Cys545Tyr(p.C545Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341164
Start	57979177:57979177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341164
Start	58000729:58000729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341164
Start	57979621:57979621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341164
Start	57979534:57979535(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1145_1146insTTTTTCTCCA
AA Mutation	p.Tyr383PhefsTer5(p.Y383Ffs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341164
Start	58001287:58001288(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.31+1dupG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF606

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978785:57978785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1895C>T
AA Mutation	p.Ser632Phe(p.S632F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978420:57978420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2260C>A
AA Mutation	p.His754Asn(p.H754N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978392:57978392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373070463
CDS Mutation	c.2288G>A
AA Mutation	p.Arg763His(p.R763H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341164
Start	57978992:57978992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1688C>A
AA Mutation	p.Ser563Tyr(p.S563Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript