Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91524243:91524243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533T>G
AA Mutation	p.Asn511Lys(p.N511K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91511794:91511794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375702482
CDS Mutation	c.443C>A
AA Mutation	p.Ser148Tyr(p.S148Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91513994:91513994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869G>T
AA Mutation	p.Arg290Ile(p.R290I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91511913:91511913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539320135
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Cys(p.R188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91515811:91515811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115C>T
AA Mutation	p.Pro372Leu(p.P372L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234626
Start	91511897:91511897(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.551delT
AA Mutation	p.Leu184TyrfsTer6(p.L184Yfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91511842:91511842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234626
Start	91511794:91511794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375702482
CDS Mutation	c.443C>A
AA Mutation	p.Ser148Tyr(p.S148Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234626
Start	91507879:91507879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141T>G
Mutation Classification	Silent
Feature Type	Transcript