Colon Cancer: Gene >> ZNF583

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56424253:56424253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775089271
CDS Mutation	c.1595G>A
AA Mutation	p.Arg532His(p.R532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56424025:56424025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367G>T
AA Mutation	p.Arg456Ile(p.R456I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423815:56423815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Lys(p.R386K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423353:56423353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>T
AA Mutation	p.Arg232Ile(p.R232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423689:56423689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031G>T
AA Mutation	p.Arg344Ile(p.R344I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56424252:56424252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769146153
CDS Mutation	c.1594C>T
AA Mutation	p.Arg532Cys(p.R532C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56424214:56424214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556C>T
AA Mutation	p.Pro519Leu(p.P519L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423521:56423521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863G>T
AA Mutation	p.Arg288Ile(p.R288I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291598
Start	56413988:56413988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000291598
Start	56423240:56423240(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770581508
CDS Mutation	c.588delA
AA Mutation	p.Lys196AsnfsTer5(p.K196Nfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000291598
Start	56423631:56423631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>T
AA Mutation	p.Glu325Ter(p.E325*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000291598
Start	56424039:56424039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381G>T
AA Mutation	p.Glu461Ter(p.E461*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF583

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423899:56423899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1241G>A
AA Mutation	p.Arg414Lys(p.R414K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56424277:56424277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619G>T
AA Mutation	p.Arg540Ile(p.R540I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423353:56423353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>T
AA Mutation	p.Arg232Ile(p.R232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423631:56423631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>A
AA Mutation	p.Glu325Lys(p.E325K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56423773:56423773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115G>T
AA Mutation	p.Arg372Ile(p.R372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000291598
Start	56424109:56424109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451G>T
AA Mutation	p.Arg484Ile(p.R484I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript