Mutation

Primary Site >> Stomach Cancer

Gene >> TRAP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3674346:3674346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037C>A
AA Mutation	p.Pro346His(p.P346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3686127:3686127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192245771
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Trp(p.R114W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3665977:3665977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1377G>T
AA Mutation	p.Glu459Asp(p.E459D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3662929:3662929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371118456
CDS Mutation	c.1747A>G
AA Mutation	p.Met583Val(p.M583V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3674427:3674427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200973932
CDS Mutation	c.956C>T
AA Mutation	p.Ala319Val(p.A319V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3674367:3674367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016T>A
AA Mutation	p.Ile339Asn(p.I339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3674365:3674365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775599442
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Cys(p.R340C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3666053:3666053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301C>T
AA Mutation	p.Ala434Val(p.A434V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3676064:3676064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786G>T
AA Mutation	p.Lys262Asn(p.K262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000246957
Start	3666110:3666110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371962678
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415Gln(p.R415Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3690885:3690885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376485209
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3689121:3689121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3663497:3663497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3658225:3658225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776747983
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3690906:3690906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3677536:3677536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246957
Start	3664316:3664316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246957
Start	3686089:3686089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.378delA
AA Mutation	p.Lys126AsnfsTer38(p.K126Nfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246957
Start	3666058:3666058(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1296delA
AA Mutation	p.Asp433MetfsTer21(p.D433Mfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000246957
Start	3672698:3672698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1165+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript