Colon Cancer: Gene >> ZNF746

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149476994:149476994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766C>A
AA Mutation	p.Leu256Ile(p.L256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149492967:149492967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767420322
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149474773:149474773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1546G>A
AA Mutation	p.Gly516Ser(p.G516S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149474629:149474629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1690C>T
AA Mutation	p.Arg564Trp(p.R564W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149494304:149494304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>T
AA Mutation	p.Gly75Val(p.G75V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149494388:149494388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149475440:149475440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879G>T
AA Mutation	p.Glu293Asp(p.E293D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149474695:149474695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1624G>A
AA Mutation	p.Glu542Lys(p.E542K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149475424:149475424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750407943
CDS Mutation	c.895G>A
AA Mutation	p.Val299Ile(p.V299I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149475302:149475302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017G>T
AA Mutation	p.Gln339His(p.Q339H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149476999:149476999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144007946
CDS Mutation	c.761C>T
AA Mutation	p.Thr254Met(p.T254M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149474751:149474751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568C>T
AA Mutation	p.Ala523Val(p.A523V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340622
Start	149494390:149494390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340622
Start	149494058:149494058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340622
Start	149474612:149474612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340622
Start	149477742:149477742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.534A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000340622
Start	149494416:149494416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112C>T
AA Mutation	p.Arg38Ter(p.R38*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF746

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340622
Start	149474419:149474419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1900A>G
AA Mutation	p.Ser634Gly(p.S634G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340622
Start	149494273:149494273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript