Colon Cancer: Gene >> ADGRF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46879862:46879862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199931272
CDS Mutation	c.992C>T
AA Mutation	p.Ser331Leu(p.S331L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46856727:46856727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3867G>T
AA Mutation	p.Gln1289His(p.Q1289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46858670:46858670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143364971
CDS Mutation	c.3233G>A
AA Mutation	p.Arg1078His(p.R1078H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46858763:46858763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3140C>T
AA Mutation	p.Ser1047Phe(p.S1047F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46863024:46863024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778170741
CDS Mutation	c.2063G>A
AA Mutation	p.Arg688Gln(p.R688Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46867075:46867075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1684G>A
AA Mutation	p.Val562Ile(p.V562I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46879884:46879884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376218074
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46859170:46859170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2733G>T
AA Mutation	p.Gln911His(p.Q911H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46868960:46868960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>T
AA Mutation	p.Arg515Ile(p.R515I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46888338:46888338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325A>G
AA Mutation	p.Thr109Ala(p.T109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46906735:46906735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28T>C
AA Mutation	p.Cys10Arg(p.C10R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46858671:46858671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3232C>T
AA Mutation	p.Arg1078Cys(p.R1078C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46858770:46858770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200682859
CDS Mutation	c.3133C>T
AA Mutation	p.Arg1045Trp(p.R1045W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46859444:46859444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2459A>T
AA Mutation	p.Asn820Ile(p.N820I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46853999:46853999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4034T>C
AA Mutation	p.Leu1345Pro(p.L1345P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46858543:46858543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748104611
CDS Mutation	c.3360T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46882090:46882090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46878296:46878296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373082410
CDS Mutation	c.1146C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46882069:46882069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46858204:46858204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3699T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46867127:46867127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199751206
CDS Mutation	c.1632C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265417
Start	46865177:46865178(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1854dupA
AA Mutation	p.Gln619ThrfsTer21(p.Q619Tfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265417
Start	46859442:46859443(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2460_2461insGCCC
AA Mutation	p.Gln821AlafsTer22(p.Q821Afs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265417
Start	46884093:46884093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46858784:46858784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372078649
CDS Mutation	c.3119C>T
AA Mutation	p.Ser1040Leu(p.S1040L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46865120:46865120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912G>T
AA Mutation	p.Val638Phe(p.V638F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46881544:46881544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725A>G
AA Mutation	p.Glu242Gly(p.E242G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46856015:46856015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3920C>A
AA Mutation	p.Ser1307Tyr(p.S1307Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46860732:46860732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2362A>C
AA Mutation	p.Asn788His(p.N788H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265417
Start	46888379:46888379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284A>C
AA Mutation	p.Asn95Thr(p.N95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46881549:46881549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265417
Start	46871934:46871934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774615419
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript