Mutation

Primary Site >> Stomach Cancer

Gene >> ABCC3

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000285238
Start	50658082:50658082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Gly163Ser(p.G163S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50665237:50665237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543738423
CDS Mutation	c.1423G>A
AA Mutation	p.Ala475Thr(p.A475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50673001:50673001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376756717
CDS Mutation	c.2272C>T
AA Mutation	p.Arg758Trp(p.R758W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50677850:50677850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3485G>A
AA Mutation	p.Arg1162Gln(p.R1162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50684815:50684815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4220T>C
AA Mutation	p.Phe1407Ser(p.F1407S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50684776:50684776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4181A>G
AA Mutation	p.Asp1394Gly(p.D1394G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50676049:50676049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3026C>T
AA Mutation	p.Ser1009Phe(p.S1009F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50655856:50655856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>A
AA Mutation	p.Glu24Lys(p.E24K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50676374:50676374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3164C>T
AA Mutation	p.Ser1055Leu(p.S1055L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50659340:50659340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778T>C
AA Mutation	p.Trp260Arg(p.W260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50668868:50668868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886T>C
AA Mutation	p.Ile629Thr(p.I629T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50687696:50687696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539211035
CDS Mutation	c.4441G>A
AA Mutation	p.Ala1481Thr(p.A1481T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000285238
Start	50684067:50684067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4073G>A
AA Mutation	p.Gly1358Asp(p.G1358D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50667610:50667610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750265761
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50665212:50665212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201511186
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50679866:50679866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373253663
CDS Mutation	c.3774G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285238
Start	50658455:50658455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191757325
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285238
Start	50658115:50658115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.521delT
AA Mutation	p.Phe174SerfsTer70(p.F174Sfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000285238
Start	50676036:50676036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3013C>T
AA Mutation	p.Gln1005Ter(p.Q1005*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285238
Start	50667967:50667968(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1744dupC
AA Mutation	p.Leu582ProfsTer31(p.L582Pfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript