Mutation

Primary Site >> Stomach Cancer

Gene >> ARHGAP21

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24620534:24620534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1361G>T
AA Mutation	p.Arg454Leu(p.R454L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24619817:24619817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078C>T
AA Mutation	p.Ala693Val(p.A693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24620264:24620264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1631C>A
AA Mutation	p.Pro544His(p.P544H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24585371:24585371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758648434
CDS Mutation	c.4918G>A
AA Mutation	p.Glu1640Lys(p.E1640K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24621084:24621084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Val271Ile(p.V271I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24620138:24620138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757T>A
AA Mutation	p.Ile586Asn(p.I586N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24622741:24622741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517A>T
AA Mutation	p.Thr173Ser(p.T173S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24596774:24596774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3443G>A
AA Mutation	p.Arg1148Gln(p.R1148Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000396432
Start	24620069:24620069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141641049
CDS Mutation	c.1826G>A
AA Mutation	p.Arg609Gln(p.R609Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396432
Start	24585795:24585795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769009600
CDS Mutation	c.4494G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396432
Start	24591899:24591899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754752303
CDS Mutation	c.3990G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396432
Start	24585873:24585873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4416C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396432
Start	24591899:24591899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3990G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396432
Start	24585108:24585108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5181A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396432
Start	24620116:24620116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1779G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396432
Start	24620958:24620958(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.937delA
AA Mutation	p.Thr313GlnfsTer17(p.T313Qfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396432
Start	24600878:24600878(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2900delG
AA Mutation	p.Gly967ValfsTer29(p.G967Vfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript