Colon Cancer: Gene >> CACNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39175243:39175243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554707348
CDS Mutation	c.1747C>T
AA Mutation	p.Arg583Cys(p.R583C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39183805:39183805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748883383
CDS Mutation	c.958G>A
AA Mutation	p.Ala320Thr(p.A320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394303
Start	39184786:39184786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Glu243Lys(p.E243K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39184127:39184127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39186549:39186549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575C>G
AA Mutation	p.Ser192Cys(p.S192C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39175639:39175639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351G>A
AA Mutation	p.Gly451Arg(p.G451R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39194904:39194904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151T>C
AA Mutation	p.Ser51Pro(p.S51P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39184801:39184801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712T>C
AA Mutation	p.Ser238Pro(p.S238P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39186810:39186810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39191579:39191579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39187554:39187554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39183755:39183755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532308568
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39184077:39184077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39197469:39197469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CACNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394303
Start	39177391:39177391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>A
AA Mutation	p.Ala431Thr(p.A431T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394303
Start	39183845:39183845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918C>T
Mutation Classification	Silent
Feature Type	Transcript