Colon Cancer: Gene >> CDC25C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138289519:138289519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909G>T
AA Mutation	p.Lys303Asn(p.K303N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138329583:138329583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259C>A
AA Mutation	p.Leu87Ile(p.L87I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138289545:138289545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766572046
CDS Mutation	c.883G>A
AA Mutation	p.Val295Met(p.V295M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138286500:138286500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200759602
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138289556:138289556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372984578
CDS Mutation	c.872C>T
AA Mutation	p.Ala291Val(p.A291V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138287180:138287180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015G>A
AA Mutation	p.Gly339Arg(p.G339R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDC25C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138286550:138286550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107G>T
AA Mutation	p.Lys369Asn(p.K369N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323760
Start	138292075:138292075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657G>T
AA Mutation	p.Glu219Asp(p.E219D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript