Colon Cancer: Gene >> CACNA2D2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50367840:50367840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2227C>T
AA Mutation	p.Arg743Cys(p.R743C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50387600:50387600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779423998
CDS Mutation	c.478G>A
AA Mutation	p.Val160Met(p.V160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50364914:50364914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770106093
CDS Mutation	c.3286C>T
AA Mutation	p.His1096Tyr(p.H1096Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50376013:50376013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1723G>A
AA Mutation	p.Val575Met(p.V575M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50365657:50365657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2968A>G
AA Mutation	p.Ile990Val(p.I990V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50367029:50367029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774552132
CDS Mutation	c.2503C>T
AA Mutation	p.Arg835Cys(p.R835C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50379532:50379532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747629573
CDS Mutation	c.1052G>A
AA Mutation	p.Arg351His(p.R351H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50379163:50379163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142559701
CDS Mutation	c.1189A>G
AA Mutation	p.Met397Val(p.M397V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50379124:50379124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763416643
CDS Mutation	c.1228G>A
AA Mutation	p.Val410Ile(p.V410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50377529:50377529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1564C>A
AA Mutation	p.Leu522Met(p.L522M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50376167:50376167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648T>C
AA Mutation	p.Phe550Leu(p.F550L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50434372:50434372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>A
AA Mutation	p.Val116Met(p.V116M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50434414:50434414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568540115
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Trp(p.R102W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000479441
Start	50375810:50375810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1844A>G
AA Mutation	p.Glu615Gly(p.E615G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50378308:50378308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760989430
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50380000:50380000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771844125
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50387580:50387580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50378976:50378976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773152404
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50379537:50379537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CACNA2D2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000479441
Start	50384276:50384276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572T>G
AA Mutation	p.Phe191Cys(p.F191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50384272:50384272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753595795
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50379976:50379976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50367063:50367063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775619000
CDS Mutation	c.2469C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479441
Start	50367874:50367874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2193C>A
Mutation Classification	Silent
Feature Type	Transcript