Mutation

Primary Site >> Stomach Cancer

Gene >> TSC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2056668:2056668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142919353
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2055424:2055424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504G>A
AA Mutation	p.Met168Ile(p.M168I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2084592:2084592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4370G>A
AA Mutation	p.Arg1457Gln(p.R1457Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2072295:2072295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182538665
CDS Mutation	c.2152C>T
AA Mutation	p.Arg718Cys(p.R718C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2074275:2074275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2431T>C
AA Mutation	p.Cys811Arg(p.C811R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2056755:2056755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45517126
CDS Mutation	c.760G>A
AA Mutation	p.Glu254Lys(p.E254K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2070493:2070493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397515063
CDS Mutation	c.1754G>A
AA Mutation	p.Arg585His(p.R585H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2056735:2056735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740T>C
AA Mutation	p.Ile247Thr(p.I247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2074282:2074282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2438T>C
AA Mutation	p.Val813Ala(p.V813A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2088461:2088461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758450326
CDS Mutation	c.5275G>A
AA Mutation	p.Ala1759Thr(p.A1759T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2088300:2088300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766093661
CDS Mutation	c.5234G>A
AA Mutation	p.Arg1745His(p.R1745H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2088051:2088051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397515110
CDS Mutation	c.5072T>C
AA Mutation	p.Met1691Thr(p.M1691T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2060800:2060800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106T>G
AA Mutation	p.Leu369Arg(p.L369R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000219476
Start	2077693:2077693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2933G>A
AA Mutation	p.Arg978His(p.R978H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2074337:2074337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773645613
CDS Mutation	c.2493G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2056664:2056664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35501344
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2071605:2071605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1935C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2070491:2070491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141285742
CDS Mutation	c.1752G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2081668:2081668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3684G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2086306:2086306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4776G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2080220:2080220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3453C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2056226:2056226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567756494
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2074373:2074373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2080301:2080301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201305783
CDS Mutation	c.3534G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2055505:2055505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397515309
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2060687:2060687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45517153
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2064385:2064385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2081647:2081647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137854268
CDS Mutation	c.3663G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219476
Start	2076083:2076083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2655C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219476
Start	2048715:2048715(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.102delA
AA Mutation	p.Lys34AsnfsTer12(p.K34Nfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript