Colon Cancer: Gene >> IFI16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159045306:159045306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339G>T
AA Mutation	p.Asp447Tyr(p.D447Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159018297:159018297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618A>G
AA Mutation	p.Ile206Met(p.I206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159032571:159032571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209G>C
AA Mutation	p.Lys403Asn(p.K403N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159020467:159020467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099T>G
AA Mutation	p.Phe367Val(p.F367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159052019:159052019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006C>T
AA Mutation	p.Ala669Val(p.A669V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159053689:159053689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2242G>T
AA Mutation	p.Gly748Trp(p.G748W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159051842:159051842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1829T>C
AA Mutation	p.Val610Ala(p.V610A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159016661:159016661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>T
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159015952:159015952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346A>C
AA Mutation	p.Lys116Gln(p.K116Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159014901:159014901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>T
AA Mutation	p.Thr74Met(p.T74M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159051926:159051926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758208458
CDS Mutation	c.1913G>A
AA Mutation	p.Arg638His(p.R638H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159051848:159051848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746538717
CDS Mutation	c.1835G>A
AA Mutation	p.Arg612Gln(p.R612Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159018351:159018351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672G>T
AA Mutation	p.Glu224Asp(p.E224D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159045451:159045451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1484G>A
AA Mutation	p.Ser495Asn(p.S495N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159051711:159051711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777391755
CDS Mutation	c.1698A>C
AA Mutation	p.Glu566Asp(p.E566D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295809
Start	159018234:159018234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370784049
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295809
Start	159051837:159051837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000295809
Start	159054900:159054900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757602743
CDS Mutation	c.*2delA
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295809
Start	159014686:159014686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.12delA
AA Mutation	p.Lys4AsnfsTer8(p.K4Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000295809
Start	159016693:159016693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542C>A
AA Mutation	p.Ser181Ter(p.S181*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000295809
Start	159020470:159020470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102C>T
AA Mutation	p.Arg368Ter(p.R368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000295809
Start	159020506:159020507(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1138_1139insACTGTTTTCTGTAA
AA Mutation	p.Ser380TyrfsTer5(p.S380Yfs*5)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295809
Start	159018351:159018352(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.679dupA
AA Mutation	p.Ile227AsnfsTer42(p.I227Nfs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IFI16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159051842:159051842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1829T>C
AA Mutation	p.Val610Ala(p.V610A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295809
Start	159045380:159045380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413C>A
AA Mutation	p.Phe471Leu(p.F471L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295809
Start	159053673:159053673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2226G>A
Mutation Classification	Silent
Feature Type	Transcript