Mutation

Primary Site >> Stomach Cancer

Gene >> NLRC5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57020821:57020821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109C>T
AA Mutation	p.Pro37Ser(p.P37S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57058120:57058120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3802C>T
AA Mutation	p.Pro1268Ser(p.P1268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57033636:57033636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2510G>T
AA Mutation	p.Arg837Met(p.R837M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57023793:57023793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201268786
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Cys(p.R122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57026099:57026099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780658848
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Trp(p.R386W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57026610:57026610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667G>A
AA Mutation	p.Gly556Asp(p.G556D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57025808:57025808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>A
AA Mutation	p.Asp289Asn(p.D289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57082475:57082475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5548A>G
AA Mutation	p.Arg1850Gly(p.R1850G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57077747:57077747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755149068
CDS Mutation	c.4948G>A
AA Mutation	p.Gly1650Arg(p.G1650R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57074652:57074652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4720C>A
AA Mutation	p.Leu1574Ile(p.L1574I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57025923:57025923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980T>C
AA Mutation	p.Leu327Pro(p.L327P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57025488:57025488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767160749
CDS Mutation	c.545G>A
AA Mutation	p.Arg182His(p.R182H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57025536:57025536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593A>G
AA Mutation	p.Asp198Gly(p.D198G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262510
Start	57026514:57026514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1571T>C
AA Mutation	p.Leu524Pro(p.L524P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57025783:57025783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57037258:57037258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2775C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57026644:57026644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1701C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57076846:57076846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113401504
CDS Mutation	c.4779C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57025561:57025561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752886380
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57026614:57026614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1671C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262510
Start	57020721:57020721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262510
Start	57026327:57026328(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1385_1386delAG
AA Mutation	p.Glu462GlyfsTer92(p.E462Gfs*92)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262510
Start	57026284:57026284(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1346delC
AA Mutation	p.Pro449LeufsTer17(p.P449Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262510
Start	57079286:57079289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5234_5237delTAGA
AA Mutation	p.Ile1745ThrfsTer27(p.I1745Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262510
Start	57054824:57054824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3584delA
AA Mutation	p.Lys1195ArgfsTer38(p.K1195Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000262510
Start	57061646:57061646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4099C>T
AA Mutation	p.Gln1367Ter(p.Q1367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000262510
Start	57066586:57066586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4294G>T
AA Mutation	p.Glu1432Ter(p.E1432*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262510
Start	57026283:57026284(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs772651939
CDS Mutation	c.1346dupC
AA Mutation	p.Gly450TrpfsTer105(p.G450Wfs*105)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262510
Start	57047581:57047582(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3375_3376insT
AA Mutation	p.Arg1126SerfsTer20(p.R1126Sfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262510
Start	57061446:57061446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3987-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	31
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000262510
Start	57037233:57037265(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2750_2782delGTGTGCTGAGGGCCGTGAGTGCGTGCTGGACCC
AA Mutation	p.Cys917_Thr927del(p.C917_T927del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript