Colon Cancer: Gene >> ADCY4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24322137:24322137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2515C>T
AA Mutation	p.Arg839Trp(p.R839W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24324176:24324176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1932G>T
AA Mutation	p.Lys644Asn(p.K644N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24322156:24322156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2496G>T
AA Mutation	p.Glu832Asp(p.E832D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24323380:24323380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2121G>T
AA Mutation	p.Trp707Cys(p.W707C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310677
Start	24326300:24326300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76097666
CDS Mutation	c.1567C>T
AA Mutation	p.Arg523Trp(p.R523W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24324365:24324365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1850G>A
AA Mutation	p.Ser617Asn(p.S617N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24326160:24326160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199640938
CDS Mutation	c.1574G>A
AA Mutation	p.Arg525His(p.R525H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24319103:24319103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780875775
CDS Mutation	c.2951G>A
AA Mutation	p.Arg984Gln(p.R984Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24324384:24324384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831G>A
AA Mutation	p.Ala611Thr(p.A611T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24318447:24318447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3203G>A
AA Mutation	p.Arg1068Gln(p.R1068Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24332577:24332577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542980474
CDS Mutation	c.464T>C
AA Mutation	p.Val155Ala(p.V155A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310677
Start	24332900:24332900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248A>G
AA Mutation	p.Gln83Arg(p.Q83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310677
Start	24330260:24330260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310677
Start	24318509:24318509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3141T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310677
Start	24318738:24318738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2997C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310677
Start	24322111:24322111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2541T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310677
Start	24326152:24326152(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746788867
CDS Mutation	c.1582delC
AA Mutation	p.Arg528GlyfsTer3(p.R528Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADCY4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310677
Start	24329530:24329530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000310677
Start	24319867:24319867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2608G>T
AA Mutation	p.Glu870Ter(p.E870*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000310677
Start	24331207:24331207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript