Mutation

Primary Site >> Stomach Cancer

Gene >> ABCC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99830372:99830372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377107178
CDS Mutation	c.2686G>A
AA Mutation	p.Glu896Lys(p.E896K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99831994:99831994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3121G>T
AA Mutation	p.Ala1041Ser(p.A1041S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99830415:99830415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149359610
CDS Mutation	c.2729G>A
AA Mutation	p.Arg910His(p.R910H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370449
Start	99804272:99804272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1463A>G
AA Mutation	p.Gln488Arg(p.Q488R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99800428:99800428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1074G>C
AA Mutation	p.Trp358Cys(p.W358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99831738:99831738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775253982
CDS Mutation	c.3011C>T
AA Mutation	p.Thr1004Ile(p.T1004I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99846997:99846997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4183C>T
AA Mutation	p.Leu1395Phe(p.L1395F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99793920:99793920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497G>A
AA Mutation	p.Cys166Tyr(p.C166Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99819212:99819212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2563T>A
AA Mutation	p.Phe855Ile(p.F855I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99797242:99797242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370287805
CDS Mutation	c.778C>T
AA Mutation	p.Arg260Trp(p.R260W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99846970:99846970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4156C>A
AA Mutation	p.Leu1386Met(p.L1386M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99836238:99836238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3562G>A
AA Mutation	p.Val1188Met(p.V1188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99807487:99807487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634T>C
AA Mutation	p.Val545Ala(p.V545A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99831992:99831992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754501570
CDS Mutation	c.3119T>C
AA Mutation	p.Ile1040Thr(p.I1040T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99817361:99817361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2148G>T
AA Mutation	p.Lys716Asn(p.K716N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000370449
Start	99800445:99800445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091C>T
AA Mutation	p.Ala364Val(p.A364V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370449
Start	99830734:99830734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2766G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370449
Start	99805396:99805396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1479G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370449
Start	99799222:99799222(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.890delA
AA Mutation	p.Lys297ArgfsTer14(p.K297Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000370449
Start	99831632:99831632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2905G>T
AA Mutation	p.Glu969Ter(p.E969*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000370449
Start	99830852:99830852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript