Mutation

Primary Site >> Liver Cancer

Gene >> MUC16

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8949505:8949505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27265A>C
AA Mutation	p.Thr9089Pro(p.T9089P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8947347:8947347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29423C>T
AA Mutation	p.Pro9808Leu(p.P9808L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8975863:8975863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5276A>T
AA Mutation	p.Asp1759Val(p.D1759V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8973871:8973871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7268A>C
AA Mutation	p.Asn2423Thr(p.N2423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8960980:8960980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15790T>G
AA Mutation	p.Ser5264Ala(p.S5264A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8888797:8888797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40702T>C
AA Mutation	p.Tyr13568His(p.Y13568H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8962128:8962128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14642A>C
AA Mutation	p.Lys4881Thr(p.K4881T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8939220:8939220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31735A>G
AA Mutation	p.Arg10579Gly(p.R10579G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8945769:8945769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31001C>T
AA Mutation	p.Ser10334Phe(p.S10334F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8955756:8955756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21014T>G
AA Mutation	p.Leu7005Trp(p.L7005W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8963335:8963335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13435C>A
AA Mutation	p.Pro4479Thr(p.P4479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8956020:8956020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20750T>A
AA Mutation	p.Met6917Lys(p.M6917K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8932777:8932777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36076C>A
AA Mutation	p.His12026Asn(p.H12026N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8883502:8883502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41507G>T
AA Mutation	p.Gly13836Val(p.G13836V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8951505:8951505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25265G>A
AA Mutation	p.Ser8422Asn(p.S8422N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8848999:8848999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43457A>C
AA Mutation	p.Glu14486Ala(p.E14486A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8882760:8882760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41653C>A
AA Mutation	p.Leu13885Met(p.L13885M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8964238:8964238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12532T>C
AA Mutation	p.Ser4178Pro(p.S4178P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8951587:8951587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25183A>G
AA Mutation	p.Ile8395Val(p.I8395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8956831:8956831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19939A>G
AA Mutation	p.Ile6647Val(p.I6647V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8960584:8960584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16186A>T
AA Mutation	p.Ser5396Cys(p.S5396C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8966366:8966366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10404C>A
AA Mutation	p.Asp3468Glu(p.D3468E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8938970:8938970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31985A>T
AA Mutation	p.Asp10662Val(p.D10662V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8856087:8856087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43190C>T
AA Mutation	p.Pro14397Leu(p.P14397L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8960650:8960650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16120G>T
AA Mutation	p.Val5374Leu(p.V5374L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8960652:8960652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16118T>G
AA Mutation	p.Leu5373Arg(p.L5373R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8922938:8922938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36323G>A
AA Mutation	p.Gly12108Asp(p.G12108D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8962690:8962690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14080C>T
AA Mutation	p.Leu4694Phe(p.L4694F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8978582:8978582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2557T>A
AA Mutation	p.Ser853Thr(p.S853T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8972362:8972362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8777C>T
AA Mutation	p.Ser2926Phe(p.S2926F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8947210:8947210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777355694
CDS Mutation	c.29560G>C
AA Mutation	p.Val9854Leu(p.V9854L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8976622:8976622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4517C>T
AA Mutation	p.Thr1506Ile(p.T1506I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8913485:8913485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37111A>T
AA Mutation	p.Thr12371Ser(p.T12371S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8937647:8937647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33308C>A
AA Mutation	p.Thr11103Asn(p.T11103N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8937648:8937648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33307A>C
AA Mutation	p.Thr11103Pro(p.T11103P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8946579:8946579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30191C>A
AA Mutation	p.Thr10064Lys(p.T10064K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8974703:8974703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6436C>T
AA Mutation	p.Leu2146Phe(p.L2146F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8949303:8949303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27467C>A
AA Mutation	p.Ser9156Tyr(p.S9156Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8973356:8973356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7783A>T
AA Mutation	p.Ser2595Cys(p.S2595C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8965434:8965434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772201780
CDS Mutation	c.11336C>G
AA Mutation	p.Ser3779Cys(p.S3779C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8909396:8909396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566860711
CDS Mutation	c.37423C>T
AA Mutation	p.Arg12475Trp(p.R12475W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8953805:8953805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22965G>T
AA Mutation	p.Gln7655His(p.Q7655H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8976503:8976503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4636A>T
AA Mutation	p.Ser1546Cys(p.S1546C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8904964:8904964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38183A>C
AA Mutation	p.Glu12728Ala(p.E12728A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8907811:8907811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780625713
CDS Mutation	c.37687C>T
AA Mutation	p.Arg12563Cys(p.R12563C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8927455:8927455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36145G>T
AA Mutation	p.Val12049Leu(p.V12049L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8937441:8937441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33514A>G
AA Mutation	p.Ile11172Val(p.I11172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	48
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8883851:8883851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41365C>G
AA Mutation	p.Leu13789Val(p.L13789V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	49
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8891882:8891882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40258C>A
AA Mutation	p.His13420Asn(p.H13420N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	50
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8976437:8976437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4702A>G
AA Mutation	p.Thr1568Ala(p.T1568A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	51
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8949618:8949618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27152C>A
AA Mutation	p.Ser9051Tyr(p.S9051Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	52
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8966076:8966076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10694A>T
AA Mutation	p.Asp3565Val(p.D3565V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	53
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8913470:8913470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37126T>A
AA Mutation	p.Ser12376Thr(p.S12376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	54
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8945547:8945547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31223G>A
AA Mutation	p.Gly10408Glu(p.G10408E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	55
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8895702:8895702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39640C>G
AA Mutation	p.Pro13214Ala(p.P13214A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	56
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8975254:8975254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5885T>A
AA Mutation	p.Met1962Lys(p.M1962K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	57
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8910111:8910111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37315G>T
AA Mutation	p.Gly12439Cys(p.G12439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	58
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8963458:8963458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13312G>A
AA Mutation	p.Asp4438Asn(p.D4438N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	59
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8953068:8953068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23702C>A
AA Mutation	p.Ala7901Glu(p.A7901E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	60
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8927406:8927406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36194C>A
AA Mutation	p.Ser12065Tyr(p.S12065Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	61
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8964118:8964118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12652C>T
AA Mutation	p.Pro4218Ser(p.P4218S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	62
Mutation Consequence	missense_variant
Transcription ID	ENST00000397910
Start	8975318:8975318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752320719
CDS Mutation	c.5821A>T
AA Mutation	p.Ile1941Phe(p.I1941F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	63
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8957816:8957816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18954T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	64
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8949881:8949881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26889C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	65
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8954912:8954912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21858T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	66
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8900785:8900785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38772T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	67
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8915566:8915566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36744T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	68
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8956499:8956499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20271T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	69
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8958518:8958518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771268392
CDS Mutation	c.18252C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	70
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8963615:8963615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13155G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	71
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8955104:8955104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21666T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	72
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8963873:8963873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12897T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	73
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8951651:8951651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25119A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	74
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8971914:8971914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9225T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	75
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8952809:8952809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23961C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	76
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8950580:8950580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26190T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	77
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8972493:8972493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8646T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	78
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8949053:8949053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27717C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	79
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8965049:8965049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11721G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	80
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8935123:8935123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35832C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	81
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8976570:8976570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4569C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	82
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8946896:8946896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29874C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	83
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8946821:8946821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29949C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	84
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8917585:8917585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36531C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	85
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397910
Start	8936869:8936869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34086C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	86
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397910
Start	8935174:8935177(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.35778_35781delAACT
AA Mutation	p.Thr11927GlnfsTer16(p.T11927Qfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	87
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8962146:8962146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14624C>A
AA Mutation	p.Ser4875Ter(p.S4875*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	88
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8938869:8938869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32086A>T
AA Mutation	p.Arg10696Ter(p.R10696*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	89
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8978238:8978238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2901G>A
AA Mutation	p.Trp967Ter(p.W967*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	90
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8937393:8937393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33562G>T
AA Mutation	p.Glu11188Ter(p.E11188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	91
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8981089:8981089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50T>A
AA Mutation	p.Leu17Ter(p.L17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	92
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8946526:8946526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30244G>T
AA Mutation	p.Glu10082Ter(p.E10082*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	93
Mutation Consequence	stop_gained
Transcription ID	ENST00000397910
Start	8963602:8963602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13168C>T
AA Mutation	p.Gln4390Ter(p.Q4390*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript