Mutation

Primary Site >> Stomach Cancer

Gene >> MCC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113043546:113043546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170A>G
AA Mutation	p.Thr724Ala(p.T724A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113064059:113064059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568G>A
AA Mutation	p.Ser523Asn(p.S523N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113071183:113071183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266G>T
AA Mutation	p.Glu422Asp(p.E422D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113053827:113053827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1776C>A
AA Mutation	p.Ser592Arg(p.S592R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113071217:113071217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232A>G
AA Mutation	p.Lys411Arg(p.K411R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302475
Start	113053727:113053727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1876A>G
AA Mutation	p.Lys626Glu(p.K626E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113085231:113085231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765539734
CDS Mutation	c.908G>A
AA Mutation	p.Arg303His(p.R303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000408903
Start	113385067:113385067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316A>G
AA Mutation	p.Lys106Glu(p.K106E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113151338:113151338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>G
AA Mutation	p.Leu48Val(p.L48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113053751:113053751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1852C>T
AA Mutation	p.Leu618Phe(p.L618F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113084179:113084179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.987G>T
AA Mutation	p.Arg329Ser(p.R329S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113064039:113064039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374053773
CDS Mutation	c.1588G>A
AA Mutation	p.Val530Met(p.V530M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113064035:113064035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1592C>T
AA Mutation	p.Ala531Val(p.A531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113082928:113082928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113028993:113028993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113028972:113028972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139931717
CDS Mutation	c.2271A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113143262:113143262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370838410
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302475
Start	113151328:113151328(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.152delA
AA Mutation	p.Lys51ArgfsTer14(p.K51Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000302475
Start	113085286:113085286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746372386
CDS Mutation	c.853C>T
AA Mutation	p.Gln285Ter(p.Q285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000408903
Start	113340545:113340545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>T
AA Mutation	p.Gly201Ter(p.G201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000302475
Start	113068081:113068082(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1457dupC
AA Mutation	p.Gly487TrpfsTer7(p.G487Wfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript