Colon Cancer: Gene >> CAMK2D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113537349:113537349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>T
AA Mutation	p.Ala170Val(p.A170V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113552083:113552083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>C
AA Mutation	p.Glu97Gln(p.E97Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113609203:113609203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113513354:113513354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920C>T
AA Mutation	p.Thr307Ile(p.T307I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113457542:113457542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226C>G
AA Mutation	p.Pro409Arg(p.P409R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113457543:113457543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1225C>T
AA Mutation	p.Pro409Ser(p.P409S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113457403:113457403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365G>T
AA Mutation	p.Trp455Cys(p.W455C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342666
Start	113460235:113460235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000342666
Start	113457462:113457462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306C>T
AA Mutation	p.Gln436Ter(p.Q436*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342666
Start	113457403:113457404(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1363_1364dupTG
AA Mutation	p.Trp455CysfsTer49(p.W455Cfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CAMK2D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113457411:113457411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357C>A
AA Mutation	p.Arg453Ser(p.R453S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342666
Start	113548717:113548717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354G>T
AA Mutation	p.Gln118His(p.Q118H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript