Colon Cancer: Gene >> ZNF839

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102341725:102341725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1982A>T
AA Mutation	p.Asp661Val(p.D661V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102339220:102339220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373766097
CDS Mutation	c.1576G>A
AA Mutation	p.Ala526Thr(p.A526T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102331761:102331761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983A>G
AA Mutation	p.Gln328Arg(p.Q328R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102326346:102326346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302T>C
AA Mutation	p.Val101Ala(p.V101A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102334635:102334635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1150C>A
AA Mutation	p.Leu384Ile(p.L384I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102326819:102326819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746395461
CDS Mutation	c.775C>T
AA Mutation	p.Pro259Ser(p.P259S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558850
Start	102331717:102331717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766689468
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558850
Start	102341996:102341996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749531935
CDS Mutation	c.2253C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558850
Start	102339207:102339207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000558850
Start	102342046:102342047(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2303_2304delAG
AA Mutation	p.Gln768ArgfsTer33(p.Q768Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF839

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000558850
Start	102334644:102334644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159A>G
AA Mutation	p.Lys387Glu(p.K387E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102331809:102331809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031A>T
AA Mutation	p.Glu344Val(p.E344V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000558850
Start	102326627:102326627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583A>G
AA Mutation	p.Lys195Glu(p.K195E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558850
Start	102326317:102326317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	start_lost
Transcription ID	ENST00000558850
Start	102326047:102326047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript