Colon Cancer: Gene >> ZNF420

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128774:37128774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1783G>T
AA Mutation	p.Ala595Ser(p.A595S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128447:37128447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775994644
CDS Mutation	c.1456C>T
AA Mutation	p.Arg486Cys(p.R486C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128061:37128061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070A>G
AA Mutation	p.His357Arg(p.H357R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128895:37128895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1904G>T
AA Mutation	p.Arg635Ile(p.R635I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37127495:37127495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504A>T
AA Mutation	p.Glu168Asp(p.E168D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128823:37128823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Gly611Asp(p.G611D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128916:37128916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925C>T
AA Mutation	p.Pro642Leu(p.P642L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37127334:37127334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Asp115Asn(p.D115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128578:37128578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587A>C
AA Mutation	p.Lys529Asn(p.K529N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128688:37128688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697A>C
AA Mutation	p.Lys566Thr(p.K566T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128175:37128175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184A>G
AA Mutation	p.Glu395Gly(p.E395G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337995
Start	37127987:37127987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337995
Start	37128070:37128070(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1083delA
AA Mutation	p.Lys361AsnfsTer214(p.K361Nfs*214)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF420

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128439:37128439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448C>A
AA Mutation	p.Ser483Tyr(p.S483Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128147:37128147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156A>G
AA Mutation	p.Thr386Ala(p.T386A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128543:37128543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1552C>A
AA Mutation	p.Leu518Ile(p.L518I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337995
Start	37128979:37128979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140027212
CDS Mutation	c.1988G>T
AA Mutation	p.Arg663Ile(p.R663I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000337995
Start	37090999:37090999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565522437
CDS Mutation	c.14T>G
AA Mutation	p.Leu5Ter(p.L5*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript