Mutation

Primary Site >> Stomach Cancer

Gene >> ARID4B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235182454:235182454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773274229
CDS Mutation	c.2465G>A
AA Mutation	p.Arg822His(p.R822H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235196111:235196111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1846G>A
AA Mutation	p.Asp616Asn(p.D616N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235182387:235182387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2532G>T
AA Mutation	p.Glu844Asp(p.E844D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235181704:235181704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3215A>G
AA Mutation	p.Asp1072Gly(p.D1072G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235181968:235181968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2951T>C
AA Mutation	p.Leu984Pro(p.L984P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235213849:235213849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1761G>T
AA Mutation	p.Met587Ile(p.M587I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235213852:235213852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758A>C
AA Mutation	p.Lys586Asn(p.K586N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235182781:235182781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2138C>A
AA Mutation	p.Ser713Tyr(p.S713Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235181904:235181904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3015T>G
AA Mutation	p.Asn1005Lys(p.N1005K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235240402:235240402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496A>T
AA Mutation	p.Arg166Trp(p.R166W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235257213:235257213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130C>A
AA Mutation	p.His44Asn(p.H44N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235257215:235257215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128G>T
AA Mutation	p.Arg43Ile(p.R43I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235172739:235172739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764887423
CDS Mutation	c.3690C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235214017:235214017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773738645
CDS Mutation	c.1593G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235182360:235182360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2559C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235182366:235182366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2553A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235229285:235229285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767085397
CDS Mutation	c.843A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235182104:235182104(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2815delA
AA Mutation	p.Thr939ArgfsTer2(p.T939Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235181918:235181918(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3001delA
AA Mutation	p.Thr1001GlnfsTer2(p.T1001Qfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235246473:235246473(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.393delT
AA Mutation	p.Phe131LeufsTer6(p.F131Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000264183
Start	235223243:235223243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Ter(p.R330*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000264183
Start	235220436:235220436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273G>T
AA Mutation	p.Glu425Ter(p.E425*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000264183
Start	235234435:235234435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Ter(p.R215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235194161:235194162(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1976dupA
AA Mutation	p.Asn659LysfsTer3(p.N659Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript