Colon Cancer: Gene >> CAMK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111394754:111394754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431C>T
AA Mutation	p.Ala144Val(p.A144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111449194:111449194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616G>T
AA Mutation	p.Gly206Trp(p.G206W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111344099:111344099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237A>C
AA Mutation	p.Lys79Asn(p.K79N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111478482:111478482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803A>G
AA Mutation	p.Glu268Gly(p.E268G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111374889:111374889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280C>A
AA Mutation	p.Leu94Ile(p.L94I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282356
Start	111224531:111224531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282356
Start	111484184:111484184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282356
Start	111224606:111224606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772865496
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282356
Start	111484073:111484073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000282356
Start	111394738:111394738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Ter(p.R139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000282356
Start	111482844:111482845(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.888_889insATCTTATTC
AA Mutation	p.Gln296_His297insIleLeuPhe(p.Q296_H297insILF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CAMK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111484228:111484228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184T>C
AA Mutation	p.Met395Thr(p.M395T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282356
Start	111374892:111374892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Cys(p.R95C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282356
Start	111482901:111482901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript