Colon Cancer: Gene >> ADCY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24820807:24820807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771914767
CDS Mutation	c.3169C>T
AA Mutation	p.Arg1057Trp(p.R1057W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24842269:24842269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941G>A
AA Mutation	p.Arg314His(p.R314H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24872677:24872677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>A
AA Mutation	p.Gly240Ser(p.G240S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24918867:24918867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121C>T
AA Mutation	p.Arg41Trp(p.R41W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24918363:24918363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Val209Met(p.V209M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24918857:24918857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131G>A
AA Mutation	p.Gly44Asp(p.G44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24820813:24820813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3163G>A
AA Mutation	p.Gly1055Arg(p.G1055R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24830717:24830717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749288972
CDS Mutation	c.2164G>A
AA Mutation	p.Val722Met(p.V722M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24918581:24918581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201922841
CDS Mutation	c.407G>A
AA Mutation	p.Arg136His(p.R136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24821618:24821618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760801151
CDS Mutation	c.3026G>A
AA Mutation	p.Arg1009His(p.R1009H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24842353:24842353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857A>C
AA Mutation	p.His286Pro(p.H286P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24828020:24828020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2314A>G
AA Mutation	p.Ser772Gly(p.S772G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24872594:24872594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>A
AA Mutation	p.Asn267Lys(p.N267K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24826100:24826100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2522C>A
AA Mutation	p.Ser841Tyr(p.S841Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918811:24918811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762088130
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24824489:24824489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540964272
CDS Mutation	c.2625C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918601:24918601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24821584:24821584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549333173
CDS Mutation	c.3060G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260600
Start	24839985:24839985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1243delG
AA Mutation	p.Val415CysfsTer27(p.V415Cfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000260600
Start	24831660:24831660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2055+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADCY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24828044:24828044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764647486
CDS Mutation	c.2290G>A
AA Mutation	p.Ala764Thr(p.A764T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24826050:24826050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761536857
CDS Mutation	c.2572C>T
AA Mutation	p.Arg858Cys(p.R858C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918436:24918436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918496:24918496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24821587:24821587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775993776
CDS Mutation	c.3057C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260600
Start	24831714:24831715(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2002dupG
AA Mutation	p.Glu668GlyfsTer22(p.E668Gfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript