Colon Cancer: Gene >> CDC25B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3802929:3802929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1214T>C
AA Mutation	p.Val405Ala(p.V405A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3803534:3803534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000245960
Start	3803536:3803536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1489A>G
AA Mutation	p.Met497Val(p.M497V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3801258:3801258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710T>A
AA Mutation	p.Leu237His(p.L237H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3797728:3797728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307T>C
AA Mutation	p.Ser103Pro(p.S103P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3804846:3804846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628G>T
AA Mutation	p.Arg543Leu(p.R543L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3804636:3804636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558T>C
AA Mutation	p.Tyr520His(p.Y520H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3802018:3802018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016C>T
AA Mutation	p.Pro339Leu(p.P339L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000245960
Start	3801050:3801050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662G>T
AA Mutation	p.Arg221Met(p.R221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245960
Start	3802034:3802034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372954698
CDS Mutation	c.1032G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245960
Start	3804645:3804645(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1569delA
AA Mutation	p.Gly524AlafsTer22(p.G524Afs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDC25B

No Mutation Annotation!