Colon Cancer: Gene >> CAMK2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44243282:44243282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569C>T
AA Mutation	p.Ala190Val(p.A190V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000395749
Start	44220826:44220826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749755008
CDS Mutation	c.1673C>T
AA Mutation	p.Ala558Val(p.A558V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44229417:44229417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201975711
CDS Mutation	c.1310C>T
AA Mutation	p.Pro437Leu(p.P437L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44247158:44247158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376C>A
AA Mutation	p.His126Asn(p.H126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44228864:44228864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773875653
CDS Mutation	c.1400A>G
AA Mutation	p.Glu467Gly(p.E467G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44234422:44234422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099A>G
AA Mutation	p.Ser367Gly(p.S367G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44220220:44220220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757820225
CDS Mutation	c.1843G>A
AA Mutation	p.Ala615Thr(p.A615T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395749
Start	44220236:44220236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1827C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395749
Start	44232831:44232831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201188394
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395749
Start	44242599:44242599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762180691
CDS Mutation	c.657G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAMK2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395749
Start	44228840:44228840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537871427
CDS Mutation	c.1424C>T
AA Mutation	p.Pro475Leu(p.P475L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript