Mutation

Primary Site >> Stomach Cancer

Gene >> SOS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39058800:39058800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218G>C
AA Mutation	p.Arg73Pro(p.R73P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39054763:39054763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Glu191Lys(p.E191K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	38995266:38995266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3203T>A
AA Mutation	p.Ile1068Asn(p.I1068N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	38986047:38986047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3779C>G
AA Mutation	p.Pro1260Arg(p.P1260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39024080:39024080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132A>T
AA Mutation	p.Thr378Ser(p.T378S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	38985952:38985952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3874G>T
AA Mutation	p.Val1292Phe(p.V1292F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39051265:39051265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775052125
CDS Mutation	c.743G>A
AA Mutation	p.Arg248His(p.R248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39035215:39035215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071G>C
AA Mutation	p.Leu357Phe(p.L357F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39010612:39010612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2482A>G
AA Mutation	p.Thr828Ala(p.T828A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000402219
Start	39051202:39051202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806T>A
AA Mutation	p.Met269Lys(p.M269K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402219
Start	39035302:39035302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778223456
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402219
Start	39022574:39022574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727505181
CDS Mutation	c.1854C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402219
Start	39012185:39012185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2331C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402219
Start	38986223:38986223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3603G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402219
Start	38995199:38995199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3270G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402219
Start	38995379:38995379(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3090delA
AA Mutation	p.Lys1030AsnfsTer6(p.K1030Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000402219
Start	38985943:38985943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3883C>T
AA Mutation	p.Arg1295Ter(p.R1295*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript