Mutation

Primary Site >> Stomach Cancer

Gene >> TLN2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62797368:62797368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6200C>T
AA Mutation	p.Ala2067Val(p.A2067V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62708710:62708710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145362831
CDS Mutation	c.2381G>A
AA Mutation	p.Arg794Gln(p.R794Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62739469:62739469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3809C>T
AA Mutation	p.Ala1270Val(p.A1270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62755544:62755544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373813759
CDS Mutation	c.4489G>A
AA Mutation	p.Ala1497Thr(p.A1497T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62647438:62647438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>T
AA Mutation	p.Thr43Ile(p.T43I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62653267:62653267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470A>G
AA Mutation	p.Glu157Gly(p.E157G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62792776:62792776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375769813
CDS Mutation	c.5872G>A
AA Mutation	p.Val1958Ile(p.V1958I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62673849:62673849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Glu271Lys(p.E271K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62762365:62762365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4873A>G
AA Mutation	p.Asn1625Asp(p.N1625D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62761684:62761684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4642C>A
AA Mutation	p.Leu1548Met(p.L1548M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000306829
Start	62653312:62653312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515A>T
AA Mutation	p.Asp172Val(p.D172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62737031:62737031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3512C>T
AA Mutation	p.Ala1171Val(p.A1171V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62805775:62805775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759956625
CDS Mutation	c.6653C>T
AA Mutation	p.Thr2218Met(p.T2218M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62722410:62722410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3049G>C
AA Mutation	p.Ala1017Pro(p.A1017P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62647341:62647341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771261514
CDS Mutation	c.31C>T
AA Mutation	p.Arg11Cys(p.R11C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62776815:62776815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5419G>A
AA Mutation	p.Ala1807Thr(p.A1807T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62736997:62736997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140997624
CDS Mutation	c.3478G>A
AA Mutation	p.Val1160Met(p.V1160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62686764:62686764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765543453
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Cys(p.R361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62711923:62711923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749680451
CDS Mutation	c.2480G>A
AA Mutation	p.Arg827His(p.R827H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62697716:62697716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201978847
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Trp(p.R441W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62781198:62781198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5573T>C
AA Mutation	p.Val1858Ala(p.V1858A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62763615:62763615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373058762
CDS Mutation	c.5014C>T
AA Mutation	p.Arg1672Trp(p.R1672W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62792771:62792771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555995247
CDS Mutation	c.5867G>A
AA Mutation	p.Arg1956His(p.R1956H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62736899:62736899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3380C>T
AA Mutation	p.Ala1127Val(p.A1127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62653308:62653308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>A
AA Mutation	p.Asp171Asn(p.D171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62657813:62657813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532505276
CDS Mutation	c.703G>A
AA Mutation	p.Glu235Lys(p.E235K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62737012:62737012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3493G>A
AA Mutation	p.Ala1165Thr(p.A1165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000306829
Start	62800729:62800729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748387093
CDS Mutation	c.6437C>T
AA Mutation	p.Ala2146Val(p.A2146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62653298:62653298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62748378:62748378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4053C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62708510:62708510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2181C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62776886:62776886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200962160
CDS Mutation	c.5490C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62716420:62716420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62697853:62697853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62776844:62776844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374140330
CDS Mutation	c.5448C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62739536:62739536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3876C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62797249:62797249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769329836
CDS Mutation	c.6081G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62702089:62702089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539209082
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62711990:62711990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2547C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62739362:62739362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367811145
CDS Mutation	c.3702G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62755588:62755588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4533C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62727153:62727153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3322C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306829
Start	62686709:62686709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767806424
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306829
Start	62776872:62776872(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5480delG
AA Mutation	p.Gly1827AlafsTer10(p.G1827Afs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	stop_gained
Transcription ID	ENST00000306829
Start	62736991:62736991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3472C>T
AA Mutation	p.Arg1158Ter(p.R1158*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	stop_gained
Transcription ID	ENST00000306829
Start	62752403:62752403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4308T>A
AA Mutation	p.Cys1436Ter(p.C1436*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	stop_gained
Transcription ID	ENST00000306829
Start	62717678:62717678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2866C>T
AA Mutation	p.Gln956Ter(p.Q956*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	48
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000306829
Start	62725105:62725105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3255+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript