Colon Cancer: Gene >> IL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81290484:81290484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364C>T
AA Mutation	p.Ala455Val(p.A455V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81303619:81303619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3389G>T
AA Mutation	p.Gly1130Val(p.G1130V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81299703:81299703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149410949
CDS Mutation	c.2377C>T
AA Mutation	p.Arg793Cys(p.R793C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81305935:81305935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3448G>T
AA Mutation	p.Ala1150Ser(p.A1150S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81292660:81292660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746485239
CDS Mutation	c.1525C>T
AA Mutation	p.Arg509Cys(p.R509C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81279573:81279573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Leu294Phe(p.L294F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81278859:81278859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833T>C
AA Mutation	p.Leu278Pro(p.L278P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81273093:81273093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>A
AA Mutation	p.Leu227Met(p.L227M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81301405:81301405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3211G>A
AA Mutation	p.Asp1071Asn(p.D1071N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81297004:81297004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979G>T
AA Mutation	p.Cys660Phe(p.C660F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81299457:81299457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781599219
CDS Mutation	c.2131G>A
AA Mutation	p.Glu711Lys(p.E711K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81300414:81300414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369121994
CDS Mutation	c.3088G>A
AA Mutation	p.Glu1030Lys(p.E1030K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81300417:81300417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3091G>T
AA Mutation	p.Asp1031Tyr(p.D1031Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81279763:81279763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070C>A
AA Mutation	p.Ser357Tyr(p.S357Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81259826:81259826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367A>T
AA Mutation	p.Ser123Cys(p.S123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81279608:81279608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377290170
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81292584:81292584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61752774
CDS Mutation	c.1449C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81225417:81225417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576209749
CDS Mutation	c.18C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81265717:81265717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764335985
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81308729:81308729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3930A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81300188:81300188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2862C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81300059:81300059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2733C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81299462:81299462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2136C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302987
Start	81300226:81300227(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2905dupC
AA Mutation	p.Leu969ProfsTer8(p.L969Pfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302987
Start	81292982:81292983(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1857_1858dupGA
AA Mutation	p.Asn620ArgfsTer67(p.N620Rfs*67)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81265705:81265705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753304539
CDS Mutation	c.468G>T
AA Mutation	p.Lys156Asn(p.K156N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81282707:81282707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780472079
CDS Mutation	c.1150G>A
AA Mutation	p.Val384Ile(p.V384I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81296980:81296980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1955G>T
AA Mutation	p.Arg652Ile(p.R652I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81225702:81225702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303C>A
AA Mutation	p.Phe101Leu(p.F101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81299861:81299861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2535C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000302987
Start	81306043:81306043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749837599
CDS Mutation	c.3556C>T
AA Mutation	p.Arg1186Ter(p.R1186*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript