Colon Cancer: Gene >> ADCY10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167878536:167878536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752239529
CDS Mutation	c.1316C>T
AA Mutation	p.Ala439Val(p.A439V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167829368:167829368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754372156
CDS Mutation	c.3649C>T
AA Mutation	p.Arg1217Cys(p.R1217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167845755:167845755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746591110
CDS Mutation	c.2815G>A
AA Mutation	p.Glu939Lys(p.E939K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167824711:167824711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3895G>A
AA Mutation	p.Ala1299Thr(p.A1299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167810838:167810838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144839993
CDS Mutation	c.4558G>A
AA Mutation	p.Val1520Ile(p.V1520I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167836403:167836403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773448816
CDS Mutation	c.3215C>T
AA Mutation	p.Ala1072Val(p.A1072V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167845653:167845653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2917A>G
AA Mutation	p.Ile973Val(p.I973V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167833045:167833045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749299065
CDS Mutation	c.3535G>A
AA Mutation	p.Glu1179Lys(p.E1179K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167823037:167823037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4139T>C
AA Mutation	p.Phe1380Ser(p.F1380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167829344:167829344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3673T>G
AA Mutation	p.Phe1225Val(p.F1225V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167861018:167861018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1662C>A
AA Mutation	p.Phe554Leu(p.F554L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167833046:167833046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3534C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167846259:167846259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2442C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167845756:167845756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141483140
CDS Mutation	c.2814C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167859813:167859813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1890G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167870355:167870355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167824739:167824739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748557475
CDS Mutation	c.3867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167845615:167845615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368950665
CDS Mutation	c.2955C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167896668:167896668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.666delC
AA Mutation	p.Asn223IlefsTer27(p.N223Ifs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167809721:167809721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4790delA
AA Mutation	p.Asn1597ThrfsTer4(p.N1597Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167854433:167854433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2228delA
AA Mutation	p.Asn743ThrfsTer33(p.N743Tfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167856362:167856374(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1962_1974delGAGATTTATGGAG
AA Mutation	p.Trp654Ter(p.W654*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000367851
Start	167901773:167901773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768185604
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Ter(p.R109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000367851
Start	167854437:167854437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2224A>T
AA Mutation	p.Lys742Ter(p.K742*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000367851
Start	167836533:167836533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3085G>T
AA Mutation	p.Glu1029Ter(p.E1029*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167837262:167837263(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764365704
CDS Mutation	c.3063dupT
AA Mutation	p.Pro1022SerfsTer2(p.P1022Sfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167905048:167905049(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.92dupC
AA Mutation	p.Glu32ArgfsTer9(p.E32Rfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000367851
Start	167845561:167845561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751771991
CDS Mutation	c.3007+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000367851
Start	167905116:167905117(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.24_25insAACAAACAT
AA Mutation	p.Phe8_Gln9insAsnLysHis(p.F8_Q9insNKH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADCY10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167870370:167870370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503G>T
AA Mutation	p.Lys501Asn(p.K501N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167836507:167836507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3111C>A
AA Mutation	p.Phe1037Leu(p.F1037L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167896688:167896688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646A>G
AA Mutation	p.Asn216Asp(p.N216D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167818209:167818209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749690491
CDS Mutation	c.4345C>A
AA Mutation	p.Leu1449Ile(p.L1449I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167836509:167836509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3109T>G
AA Mutation	p.Phe1037Val(p.F1037V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167880158:167880158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173C>A
Mutation Classification	Silent
Feature Type	Transcript