Mutation

Primary Site >> Stomach Cancer

Gene >> XIRP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39188946:39188946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>C
AA Mutation	p.Glu167Ala(p.E167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39189282:39189282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150061276
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39184666:39184666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376296366
CDS Mutation	c.4780G>A
AA Mutation	p.Ala1594Thr(p.A1594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186036:39186036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3410C>T
AA Mutation	p.Thr1137Ile(p.T1137I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187752:39187752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752430488
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565Gln(p.R565Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187942:39187942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504G>A
AA Mutation	p.Glu502Lys(p.E502K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39185752:39185752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3694G>T
AA Mutation	p.Gly1232Cys(p.G1232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186438:39186438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745985294
CDS Mutation	c.3008C>T
AA Mutation	p.Pro1003Leu(p.P1003L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39189163:39189163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753453159
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Cys(p.R95C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186024:39186024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3422G>T
AA Mutation	p.Gly1141Val(p.G1141V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187149:39187149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2297G>A
AA Mutation	p.Ser766Asn(p.S766N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39185769:39185769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3677T>C
AA Mutation	p.Leu1226Pro(p.L1226P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39189136:39189136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Asp104Asn(p.D104N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187414:39187414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116921702
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Trp(p.R678W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39185049:39185049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4397G>C
AA Mutation	p.Arg1466Thr(p.R1466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39188412:39188412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034A>G
AA Mutation	p.Gln345Arg(p.Q345R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39184242:39184242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5204C>A
AA Mutation	p.Pro1735His(p.P1735H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39185268:39185268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4178G>A
AA Mutation	p.Gly1393Glu(p.G1393E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39185911:39185911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3535C>T
AA Mutation	p.Arg1179Cys(p.R1179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39188346:39188346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764723781
CDS Mutation	c.1100C>T
AA Mutation	p.Ala367Val(p.A367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186597:39186597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2849C>T
AA Mutation	p.Ala950Val(p.A950V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39189280:39189280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752930588
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Cys(p.R56C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39187706:39187706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39186082:39186082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3364A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39186671:39186671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149549006
CDS Mutation	c.2775C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188387:39188387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6790392
CDS Mutation	c.1059G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188255:39188255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39187073:39187073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2373C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188990:39188990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200486615
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39189440:39189440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755310715
CDS Mutation	c.6C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39186005:39186005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745587316
CDS Mutation	c.3441C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39189416:39189416(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.30delC
AA Mutation	p.Thr11HisfsTer4(p.T11Hfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39187810:39187810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1636delG
AA Mutation	p.Asp546ThrfsTer16(p.D546Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39186044:39186044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3402delG
AA Mutation	p.Trp1135GlyfsTer2(p.W1135Gfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39185853:39185853(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3593delG
AA Mutation	p.Gly1198AlafsTer29(p.G1198Afs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000340369
Start	39185104:39185104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4342C>T
AA Mutation	p.Gln1448Ter(p.Q1448*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript