Mutation

Primary Site >> Stomach Cancer

Gene >> IL16

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81299906:81299906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2580G>T
AA Mutation	p.Gln860His(p.Q860H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81300106:81300106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750738616
CDS Mutation	c.2780G>A
AA Mutation	p.Arg927Gln(p.R927Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302987
Start	81303649:81303649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373703375
CDS Mutation	c.3419C>T
AA Mutation	p.Thr1140Met(p.T1140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81306139:81306139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3652G>A
AA Mutation	p.Ala1218Thr(p.A1218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81299547:81299547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2221A>G
AA Mutation	p.Asn741Asp(p.N741D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81300145:81300145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372666112
CDS Mutation	c.2819C>T
AA Mutation	p.Pro940Leu(p.P940L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81300281:81300281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2955C>A
AA Mutation	p.Ser985Arg(p.S985R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81292636:81292636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501C>G
AA Mutation	p.Arg501Gly(p.R501G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
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

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81282693:81282693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1136T>C
AA Mutation	p.Ile379Thr(p.I379T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81301379:81301379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149220649
CDS Mutation	c.3185C>T
AA Mutation	p.Thr1062Met(p.T1062M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81308691:81308691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3892T>G
AA Mutation	p.Phe1298Val(p.F1298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81293023:81293023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1888C>A
AA Mutation	p.Pro630Thr(p.P630T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302987
Start	81279748:81279748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055T>C
AA Mutation	p.Ile352Thr(p.I352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81282745:81282745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556598858
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81290470:81290470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81296999:81296999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201624502
CDS Mutation	c.1974C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81273149:81273149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753530668
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81285767:81285767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746045639
CDS Mutation	c.1269G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81292662:81292662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1527C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81308777:81308777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3978C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81299900:81299900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302987
Start	81292734:81292734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200203181
CDS Mutation	c.1599G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302987
Start	81300128:81300128(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2807delC
AA Mutation	p.Pro936LeufsTer7(p.P936Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000302987
Start	81299991:81299991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2665C>T
AA Mutation	p.Arg889Ter(p.R889*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000302987
Start	81292609:81292609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764346894
CDS Mutation	c.1474C>T
AA Mutation	p.Arg492Ter(p.R492*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302987
Start	81301463:81301464(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3276dupA
AA Mutation	p.Leu1093ThrfsTer10(p.L1093Tfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302987
Start	81273159:81273160(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.750dupT
AA Mutation	p.Ala251CysfsTer15(p.A251Cfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript