Mutation

Primary Site >> Stomach Cancer

Gene >> IQUB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123479881:123479881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111558568
CDS Mutation	c.1324A>G
AA Mutation	p.Thr442Ala(p.T442A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123461506:123461506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141036933
CDS Mutation	c.1858C>T
AA Mutation	p.Arg620Cys(p.R620C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123503292:123503292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604A>C
AA Mutation	p.Ile202Leu(p.I202L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123502948:123502948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760765844
CDS Mutation	c.863C>T
AA Mutation	p.Thr288Met(p.T288M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123461503:123461503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765950092
CDS Mutation	c.1861C>T
AA Mutation	p.Arg621Cys(p.R621C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123461553:123461553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1811G>T
AA Mutation	p.Cys604Phe(p.C604F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123479895:123479895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310T>C
AA Mutation	p.Leu437Pro(p.L437P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324698
Start	123479964:123479964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241G>A
AA Mutation	p.Arg414Gln(p.R414Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324698
Start	123502687:123502687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190528534
CDS Mutation	c.933T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324698
Start	123469328:123469328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324698
Start	123479801:123479802(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1403dupT
AA Mutation	p.Leu468PhefsTer3(p.L468Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324698
Start	123464859:123464860(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1731dupT
AA Mutation	p.Asn578Ter(p.N578*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript