Mutation

Primary Site >> Stomach Cancer

Gene >> TRRAP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98971845:98971845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76587346
CDS Mutation	c.7718C>T
AA Mutation	p.Thr2573Met(p.T2573M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98949469:98949469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4820A>T
AA Mutation	p.Asn1607Ile(p.N1607I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98955252:98955252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5864A>G
AA Mutation	p.His1955Arg(p.H1955R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98892482:98892482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98906249:98906249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109C>T
AA Mutation	p.Thr370Ile(p.T370I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98984198:98984198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9140T>A
AA Mutation	p.Ile3047Asn(p.I3047N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98893817:98893817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386T>C
AA Mutation	p.Val129Ala(p.V129A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98921762:98921762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201802078
CDS Mutation	c.2632C>T
AA Mutation	p.Arg878Cys(p.R878C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	99012124:99012124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11349A>C
AA Mutation	p.Lys3783Asn(p.K3783N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98948318:98948318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4625C>T
AA Mutation	p.Thr1542Met(p.T1542M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98933397:98933397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4009A>G
AA Mutation	p.Thr1337Ala(p.T1337A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98971939:98971939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7812G>T
AA Mutation	p.Glu2604Asp(p.E2604D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	99011200:99011200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11045C>T
AA Mutation	p.Ala3682Val(p.A3682V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	99012114:99012114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560766520
CDS Mutation	c.11339C>T
AA Mutation	p.Ala3780Val(p.A3780V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98959426:98959426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149626121
CDS Mutation	c.6404G>A
AA Mutation	p.Arg2135Gln(p.R2135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98925235:98925235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2947G>A
AA Mutation	p.Ala983Thr(p.A983T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98915745:98915745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2222A>T
AA Mutation	p.Asn741Ile(p.N741I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98911105:98911105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1841A>G
AA Mutation	p.Tyr614Cys(p.Y614C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	99011196:99011196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11041T>G
AA Mutation	p.Phe3681Val(p.F3681V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98915804:98915804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2281C>T
AA Mutation	p.Arg761Trp(p.R761W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98967549:98967549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7342C>T
AA Mutation	p.Arg2448Cys(p.R2448C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98915776:98915776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2253G>T
AA Mutation	p.Lys751Asn(p.K751N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98953425:98953425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5701G>A
AA Mutation	p.Val1901Ile(p.V1901I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98970143:98970143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7523C>G
AA Mutation	p.Pro2508Arg(p.P2508R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98937191:98937191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4147A>G
AA Mutation	p.Arg1383Gly(p.R1383G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98976173:98976173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201145010
CDS Mutation	c.7843G>A
AA Mutation	p.Val2615Ile(p.V2615I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98988874:98988874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778465879
CDS Mutation	c.9511C>T
AA Mutation	p.Arg3171Trp(p.R3171W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98967589:98967589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7382T>G
AA Mutation	p.Val2461Gly(p.V2461G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	99011097:99011097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10942C>T
AA Mutation	p.Arg3648Cys(p.R3648C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98893810:98893810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379G>A
AA Mutation	p.Glu127Lys(p.E127K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98899740:98899740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773T>C
AA Mutation	p.Ile258Thr(p.I258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98949739:98949739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5012G>T
AA Mutation	p.Trp1671Leu(p.W1671L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98959356:98959356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6334A>G
AA Mutation	p.Thr2112Ala(p.T2112A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98953352:98953352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5628C>G
AA Mutation	p.Asp1876Glu(p.D1876E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98921828:98921828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2698G>A
AA Mutation	p.Gly900Ser(p.G900S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98949747:98949747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5020G>C
AA Mutation	p.Glu1674Gln(p.E1674Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	99012323:99012323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11548C>T
AA Mutation	p.Arg3850Cys(p.R3850C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98981907:98981907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8752G>A
AA Mutation	p.Glu2918Lys(p.E2918K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98897774:98897774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782040657
CDS Mutation	c.541G>A
AA Mutation	p.Glu181Lys(p.E181K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98921771:98921771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375735930
CDS Mutation	c.2641C>T
AA Mutation	p.Arg881Cys(p.R881C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98927258:98927258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3067A>C
AA Mutation	p.Thr1023Pro(p.T1023P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98955105:98955105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5717A>G
AA Mutation	p.His1906Arg(p.H1906R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98976646:98976646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755078580
CDS Mutation	c.8102A>G
AA Mutation	p.Asn2701Ser(p.N2701S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98948609:98948609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4691G>A
AA Mutation	p.Arg1564Gln(p.R1564Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98911244:98911244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980G>T
AA Mutation	p.Glu660Asp(p.E660D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98949817:98949817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5090C>T
AA Mutation	p.Ala1697Val(p.A1697V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98970176:98970176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772886903
CDS Mutation	c.7556C>T
AA Mutation	p.Pro2519Leu(p.P2519L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	48
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98908828:98908828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216A>G
AA Mutation	p.Ile406Val(p.I406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	49
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98961441:98961441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6649T>C
AA Mutation	p.Ser2217Pro(p.S2217P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	50
Mutation Consequence	missense_variant
Transcription ID	ENST00000359863
Start	98925206:98925206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2918C>T
AA Mutation	p.Ala973Val(p.A973V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	99012250:99012250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762119583
CDS Mutation	c.11475C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98976557:98976557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202052450
CDS Mutation	c.8013G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98956178:98956178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5949G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98967647:98967647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55747560
CDS Mutation	c.7440G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	99008435:99008435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10770A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98976665:98976665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773244623
CDS Mutation	c.8121G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98976761:98976761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8217G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	58
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98983407:98983407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148646770
CDS Mutation	c.8949C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	59
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98993695:98993695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9963C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	60
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	99004296:99004296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10374C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	61
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98927263:98927263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782364391
CDS Mutation	c.3072C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	62
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98945764:98945764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781786758
CDS Mutation	c.4491C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	63
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98965781:98965781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7041C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	64
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	99011096:99011096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10941G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	65
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98937733:98937733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4317C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	66
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98984328:98984328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9270A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	67
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98984178:98984178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746931138
CDS Mutation	c.9120G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	68
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98983353:98983353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533514905
CDS Mutation	c.8895C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	69
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	99011481:99011481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140449855
CDS Mutation	c.11241G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	70
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98948583:98948583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4665A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	71
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	99012202:99012202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11427C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	72
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98953286:98953286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5562C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	73
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359863
Start	98988891:98988891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372255507
CDS Mutation	c.9528C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	74
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359863
Start	98949500:98949500(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4856delG
AA Mutation	p.Gly1619ValfsTer28(p.G1619Vfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	75
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359863
Start	98930713:98930713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3479delG
AA Mutation	p.Gly1160ValfsTer25(p.G1160Vfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	76
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359863
Start	99012086:99012086(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.11314delA
AA Mutation	p.Thr3772ArgfsTer48(p.T3772Rfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	77
Mutation Consequence	stop_gained
Transcription ID	ENST00000359863
Start	98949729:98949729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5002C>T
AA Mutation	p.Arg1668Ter(p.R1668*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	78
Mutation Consequence	stop_gained
Transcription ID	ENST00000359863
Start	99011449:99011449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11209G>T
AA Mutation	p.Glu3737Ter(p.E3737*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	79
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359863
Start	98970265:98970266(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.7648dupG
AA Mutation	p.Glu2550GlyfsTer93(p.E2550Gfs*93)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	80
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359863
Start	99012121:99012122(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.11353dupA
AA Mutation	p.Thr3785AsnfsTer137(p.T3785Nfs*137)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript