Colon Cancer: Gene >> CAMK2G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73847257:73847257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787G>A
AA Mutation	p.Ala263Thr(p.A263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000322680
Start	73853244:73853244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223C>T
AA Mutation	p.Arg75Cys(p.R75C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73848056:73848056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628G>T
AA Mutation	p.Gly210Cys(p.G210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73847332:73847332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712T>C
AA Mutation	p.Trp238Arg(p.W238R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73837484:73837484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974C>T
AA Mutation	p.Ser325Leu(p.S325L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73849272:73849272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403A>G
AA Mutation	p.Arg135Gly(p.R135G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73852311:73852311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284G>A
AA Mutation	p.Gly95Asp(p.G95D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73873005:73873005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761674491
CDS Mutation	c.144G>T
AA Mutation	p.Lys48Asn(p.K48N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73817551:73817551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760411599
CDS Mutation	c.1271G>A
AA Mutation	p.Arg424Gln(p.R424Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73848549:73848549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578A>C
AA Mutation	p.Lys193Thr(p.K193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73815133:73815133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1553G>A
AA Mutation	p.Gly518Glu(p.G518E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73815191:73815191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495G>A
AA Mutation	p.Val499Met(p.V499M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73815176:73815176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510G>A
AA Mutation	p.Ala504Thr(p.A504T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73817509:73817509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1313C>G
AA Mutation	p.Ala438Gly(p.A438G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322680
Start	73824055:73824055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322680
Start	73824058:73824058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000322680
Start	73873081:73873081(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.68delG
AA Mutation	p.Gly23ValfsTer10(p.G23Vfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000322680
Start	73853247:73853247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CAMK2G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322680
Start	73817040:73817040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421A>C
AA Mutation	p.Lys474Thr(p.K474T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript