Mutation

Primary Site >> Stomach Cancer

Gene >> ABCC4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95209537:95209537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>A
AA Mutation	p.Leu228Ile(p.L228I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95074244:95074244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376326528
CDS Mutation	c.2887G>A
AA Mutation	p.Val963Ile(p.V963I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95188491:95188491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>A
AA Mutation	p.Glu439Lys(p.E439K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95062736:95062736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771698317
CDS Mutation	c.3334G>A
AA Mutation	p.Asp1112Asn(p.D1112N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95034716:95034716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3759A>T
AA Mutation	p.Lys1253Asn(p.K1253N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95206750:95206750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943T>A
AA Mutation	p.Cys315Ser(p.C315S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95207918:95207918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793A>G
AA Mutation	p.Thr265Ala(p.T265A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95186835:95186835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368213763
CDS Mutation	c.1411G>A
AA Mutation	p.Val471Met(p.V471M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95234735:95234735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>A
AA Mutation	p.Ala136Thr(p.A136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95301273:95301273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>T
AA Mutation	p.Gln14His(p.Q14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95186820:95186820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426G>A
AA Mutation	p.Ala476Thr(p.A476T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95161279:95161279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779403637
CDS Mutation	c.2365G>A
AA Mutation	p.Val789Ile(p.V789I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95247673:95247673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142182014
CDS Mutation	c.155G>A
AA Mutation	p.Arg52His(p.R52H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95161280:95161280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11568709
CDS Mutation	c.2364C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95170591:95170591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95206676:95206676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571589752
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376887
Start	95083178:95083178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2648delT
AA Mutation	p.Leu883TrpfsTer7(p.L883Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376887
Start	95043762:95043762(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs756859429
CDS Mutation	c.3655delA
AA Mutation	p.Ile1219SerfsTer11(p.I1219Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376887
Start	95083195:95083195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2631delT
AA Mutation	p.Leu878PhefsTer12(p.L878Ffs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000376887
Start	95188464:95188464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342G>T
AA Mutation	p.Gly448Ter(p.G448*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000376887
Start	95071661:95071661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3210+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript