Colon Cancer: Gene >> ZNF410

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000555044
Start	73909401:73909401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974G>A
AA Mutation	p.Ser325Asn(p.S325N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000555044
Start	73909371:73909371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>T
AA Mutation	p.Gly315Val(p.G315V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000555044
Start	73898197:73898197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515C>T
AA Mutation	p.Ala172Val(p.A172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000555044
Start	73896394:73896394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>A
AA Mutation	p.Gly83Asp(p.G83D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000555044
Start	73898240:73898240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>T
AA Mutation	p.Lys186Asn(p.K186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000555044
Start	73898111:73898111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201192028
CDS Mutation	c.429T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555044
Start	73923423:73923424(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1299_1300insTCTATTT
AA Mutation	p.Leu434SerfsTer8(p.L434Sfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF410

No Mutation Annotation!