Colon Cancer: Gene >> CDC25A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48177972:48177972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566G>T
AA Mutation	p.Arg189Ile(p.R189I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48180828:48180828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442T>C
AA Mutation	p.Phe148Leu(p.F148L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48164358:48164358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1271G>A
AA Mutation	p.Arg424His(p.R424H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48186744:48186744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206G>C
AA Mutation	p.Ser69Thr(p.S69T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48159003:48159003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506Gln(p.R506Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48184684:48184684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>T
AA Mutation	p.Asp87Tyr(p.D87Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302506
Start	48159430:48159430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302506
Start	48177884:48177884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766671573
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302506
Start	48167924:48167924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747526743
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302506
Start	48159047:48159047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302506
Start	48180766:48180766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302506
Start	48159347:48159347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302506
Start	48159372:48159372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1406delG
AA Mutation	p.Gly469AspfsTer7(p.G469Dfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000302506
Start	48159442:48159442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336A>T
AA Mutation	p.Arg446Ter(p.R446*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDC25A

No Mutation Annotation!