Colon Cancer: Gene >> CACNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18534148:18534148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127A>G
AA Mutation	p.Asp376Gly(p.D376G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18539621:18539621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758934103
CDS Mutation	c.1880G>A
AA Mutation	p.Arg627His(p.R627H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18527661:18527661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140614930
CDS Mutation	c.1018G>A
AA Mutation	p.Ala340Thr(p.A340T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18140780:18140780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44C>T
AA Mutation	p.Ala15Val(p.A15V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18538297:18538297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420C>A
AA Mutation	p.Pro474Thr(p.P474T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18538310:18538310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781646326
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478His(p.R478H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18498466:18498466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>T
AA Mutation	p.His149Tyr(p.H149Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324631
Start	18514285:18514285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324631
Start	18402029:18402029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324631
Start	18538322:18538322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1445delC
AA Mutation	p.Thr482IlefsTer10(p.T482Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CACNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18539496:18539496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1755C>G
AA Mutation	p.His585Gln(p.H585Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18534145:18534145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs578106427
CDS Mutation	c.1124C>T
AA Mutation	p.Ala375Val(p.A375V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18539716:18539716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77141223
CDS Mutation	c.1975C>T
AA Mutation	p.Arg659Cys(p.R659C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18538321:18538321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1444A>C
AA Mutation	p.Thr482Pro(p.T482P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324631
Start	18539717:18539717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780134367
CDS Mutation	c.1976G>A
AA Mutation	p.Arg659His(p.R659H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324631
Start	18538315:18538315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438T>C
Mutation Classification	Silent
Feature Type	Transcript