Colon Cancer: Gene >> ZNF292

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87260226:87260226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6597G>T
AA Mutation	p.Met2199Ile(p.M2199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87218678:87218678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485A>C
AA Mutation	p.Lys162Thr(p.K162T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87255965:87255965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336C>T
AA Mutation	p.Ala779Val(p.A779V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258206:87258206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200259538
CDS Mutation	c.4577C>T
AA Mutation	p.Thr1526Met(p.T1526M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87259045:87259045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5416T>G
AA Mutation	p.Leu1806Val(p.L1806V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257674:87257674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199514946
CDS Mutation	c.4045C>T
AA Mutation	p.Arg1349Trp(p.R1349W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258040:87258040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4411C>T
AA Mutation	p.Pro1471Ser(p.P1471S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258564:87258564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4935A>C
AA Mutation	p.Gln1645His(p.Q1645H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87259064:87259064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5435T>G
AA Mutation	p.Phe1812Cys(p.F1812C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261736:87261736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8107G>T
AA Mutation	p.Asp2703Tyr(p.D2703Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261535:87261535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7906G>A
AA Mutation	p.Val2636Met(p.V2636M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257977:87257977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4348G>C
AA Mutation	p.Asp1450His(p.D1450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261740:87261740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8111C>A
AA Mutation	p.Pro2704Gln(p.P2704Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257260:87257260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3631A>G
AA Mutation	p.Ile1211Val(p.I1211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258304:87258304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4675T>A
AA Mutation	p.Ser1559Thr(p.S1559T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87260764:87260764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7135A>G
AA Mutation	p.Thr2379Ala(p.T2379A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87255366:87255366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737T>A
AA Mutation	p.Asn579Lys(p.N579K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261269:87261269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7640T>C
AA Mutation	p.Val2547Ala(p.V2547A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87243529:87243529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796G>A
AA Mutation	p.Glu266Lys(p.E266K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87256825:87256825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750419851
CDS Mutation	c.3196A>G
AA Mutation	p.Lys1066Glu(p.K1066E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87259708:87259708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771470765
CDS Mutation	c.6079G>A
AA Mutation	p.Ala2027Thr(p.A2027T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261470:87261470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7841A>G
AA Mutation	p.His2614Arg(p.H2614R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261777:87261777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8148A>C
AA Mutation	p.Lys2716Asn(p.K2716N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87255215:87255215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1586T>C
AA Mutation	p.Phe529Ser(p.F529S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258620:87258620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4991T>C
AA Mutation	p.Ile1664Thr(p.I1664T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87259406:87259406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5777T>G
AA Mutation	p.Ile1926Ser(p.I1926S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261267:87261267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7638A>C
AA Mutation	p.Lys2546Asn(p.K2546N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261581:87261581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7952T>G
AA Mutation	p.Phe2651Cys(p.F2651C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257753:87257753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4124T>G
AA Mutation	p.Phe1375Cys(p.F1375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257822:87257822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4193C>T
AA Mutation	p.Ser1398Phe(p.S1398F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258148:87258148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750773292
CDS Mutation	c.4519G>A
AA Mutation	p.Glu1507Lys(p.E1507K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87260702:87260702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7073C>A
AA Mutation	p.Ser2358Tyr(p.S2358Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87259055:87259055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5426C>A
AA Mutation	p.Ser1809Tyr(p.S1809Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258553:87258553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4924A>G
AA Mutation	p.Asn1642Asp(p.N1642D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87260185:87260185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370843050
CDS Mutation	c.6556A>G
AA Mutation	p.Ile2186Val(p.I2186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257819:87257819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4190G>A
AA Mutation	p.Arg1397Gln(p.R1397Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87255621:87255621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87259635:87259635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6006T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87257505:87257505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374397962
CDS Mutation	c.3876T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87255654:87255654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2025A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87261393:87261393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7764A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87257526:87257526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3897A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87256002:87256002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749843149
CDS Mutation	c.2373G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87215977:87215977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87256662:87256662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3033C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87255630:87255630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370027286
CDS Mutation	c.2001A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87260133:87260134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6505_6506delTT
AA Mutation	p.Leu2169GlufsTer9(p.L2169Efs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87218640:87218640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.452delT
AA Mutation	p.Leu151Ter(p.L151*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87255202:87255203(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1579_1580delAG
AA Mutation	p.Arg527GlyfsTer8(p.R527Gfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87261256:87261256(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7633delA
AA Mutation	p.Arg2545GlyfsTer14(p.R2545Gfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87261506:87261509(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7878_7881delTTCA
AA Mutation	p.Asn2626LysfsTer10(p.N2626Kfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87258790:87258790(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5162delT
AA Mutation	p.Leu1721Ter(p.L1721*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87258335:87258335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4710delT
AA Mutation	p.Pro1571GlnfsTer7(p.P1571Qfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	54
Mutation Consequence	stop_gained
Transcription ID	ENST00000369577
Start	87259972:87259972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6343C>T
AA Mutation	p.Arg2115Ter(p.R2115*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	55
Mutation Consequence	stop_gained
Transcription ID	ENST00000369577
Start	87260146:87260146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6517C>T
AA Mutation	p.Arg2173Ter(p.R2173*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	56
Mutation Consequence	stop_gained
Transcription ID	ENST00000369577
Start	87255211:87255211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1582G>T
AA Mutation	p.Gly528Ter(p.G528*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	57
Mutation Consequence	stop_gained
Transcription ID	ENST00000369577
Start	87261660:87261660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8031C>A
AA Mutation	p.Cys2677Ter(p.C2677*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	58
Mutation Consequence	stop_gained
Transcription ID	ENST00000369577
Start	87255277:87255277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>T
AA Mutation	p.Glu550Ter(p.E550*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	59
Mutation Consequence	stop_gained
Transcription ID	ENST00000369577
Start	87233396:87233396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>T
AA Mutation	p.Gln204Ter(p.Q204*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87255786:87255787(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2163dupA
AA Mutation	p.Val722SerfsTer7(p.V722Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	61
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87259817:87259818(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6188_6189insATTACTGTGGGTA
AA Mutation	p.Ser2064LeufsTer9(p.S2064Lfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF292

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87255226:87255226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758455764
CDS Mutation	c.1597C>T
AA Mutation	p.Arg533Trp(p.R533W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257879:87257879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4250G>A
AA Mutation	p.Gly1417Glu(p.G1417E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87258148:87258148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750773292
CDS Mutation	c.4519G>A
AA Mutation	p.Glu1507Lys(p.E1507K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87233342:87233342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556T>G
AA Mutation	p.Phe186Val(p.F186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87255707:87255707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078A>C
AA Mutation	p.Lys693Thr(p.K693T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87256958:87256958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3329A>G
AA Mutation	p.Asn1110Ser(p.N1110S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87261006:87261006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7377T>G
AA Mutation	p.Asn2459Lys(p.N2459K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87233382:87233382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596T>G
AA Mutation	p.Leu199Arg(p.L199R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87257033:87257033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3404A>C
AA Mutation	p.Lys1135Thr(p.K1135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369577
Start	87259435:87259435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5806G>A
AA Mutation	p.Glu1936Lys(p.E1936K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87218685:87218685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752923565
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87260352:87260352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367626971
CDS Mutation	c.6723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87257967:87257967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4338A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87258246:87258246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4617T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87260007:87260007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201454729
CDS Mutation	c.6378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369577
Start	87245596:87245596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372926128
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369577
Start	87257562:87257562(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3938delG
AA Mutation	p.Gly1313ValfsTer12(p.G1313Vfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript