Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02887:Nbeal1'

363854

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Nbeal1

Ensembl Gene

ENSMUSG00000073664

Gene Name

neurobeachin like 1

Synonyms

A530083I02Rik, A530050O19Rik, ALS2CR17, 2310076G13Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02887

Quality Score

Status

Chromosome

Chromosomal Location

60180599-60338328 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 60287444 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000125592 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000160834] [ENSMUST00000162291]

AlphaFold

E9PYP2

Predicted Effect

probably benign
Transcript: ENSMUST00000035569

SMART Domains

Protein: ENSMUSP00000049393
Gene: ENSMUSG00000073664

Domain	Start	End	E-Value	Type
low complexity region	522	541	N/A	INTRINSIC
low complexity region	719	735	N/A	INTRINSIC
Pfam:DUF4704	851	1130	3.4e-39	PFAM
low complexity region	1383	1401	N/A	INTRINSIC
Pfam:DUF4800	1575	1828	6.3e-126	PFAM
coiled coil region	1859	1882	N/A	INTRINSIC
Pfam:PH_BEACH	1889	1975	2e-24	PFAM
Beach	1998	2278	7.2e-199	SMART
Blast:Beach	2342	2405	6e-30	BLAST
WD40	2425	2463	5.52e-2	SMART
WD40	2475	2514	4.95e-4	SMART
WD40	2604	2649	7.64e1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000159344

SMART Domains

Protein: ENSMUSP00000124850
Gene: ENSMUSG00000073664

Domain	Start	End	E-Value	Type
Beach	31	246	4.21e-109	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000160834

SMART Domains

Protein: ENSMUSP00000124056
Gene: ENSMUSG00000073664

Domain	Start	End	E-Value	Type
low complexity region	522	541	N/A	INTRINSIC
Pfam:Laminin_G_3	567	801	8.3e-9	PFAM
low complexity region	1383	1401	N/A	INTRINSIC
low complexity region	1849	1865	N/A	INTRINSIC
Pfam:PH_BEACH	1882	1975	4.9e-32	PFAM
Beach	1998	2278	7.2e-199	SMART
Blast:Beach	2342	2405	6e-30	BLAST
WD40	2425	2463	5.52e-2	SMART
WD40	2475	2514	4.95e-4	SMART
WD40	2604	2649	7.64e1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000162291

SMART Domains

Protein: ENSMUSP00000125592
Gene: ENSMUSG00000073664

Domain	Start	End	E-Value	Type
low complexity region	114	132	N/A	INTRINSIC
low complexity region	580	596	N/A	INTRINSIC
Pfam:PH_BEACH	613	706	9.6e-33	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190958

Coding Region Coverage

Validation Efficiency

Allele List at MGI

All alleles(16) : Targeted(1) Gene trapped(15)

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017B05Rik	A	G	9: 57,258,885 (GRCm38)	Y69H	probably damaging	Het
Afap1l2	A	T	19: 56,920,563 (GRCm38)	S310R	probably damaging	Het
Aldh7a1	A	G	18: 56,542,216 (GRCm38)		probably benign	Het
Anxa8	T	A	14: 34,096,524 (GRCm38)		probably null	Het
Ap1ar	T	C	3: 127,808,543 (GRCm38)	E282G	probably damaging	Het
Arl6ip6	T	G	2: 53,202,927 (GRCm38)	S155A	probably benign	Het
Armc9	T	C	1: 86,164,835 (GRCm38)	F107S	probably damaging	Het
Ash1l	C	A	3: 88,984,181 (GRCm38)	D1122E	probably benign	Het
Atp2b4	T	A	1: 133,728,774 (GRCm38)	I713F	probably damaging	Het
BC005624	A	C	2: 30,973,305 (GRCm38)		probably benign	Het
Calcrl	T	C	2: 84,339,242 (GRCm38)	D365G	probably benign	Het
Ccdc110	A	G	8: 45,943,184 (GRCm38)	N704S	probably benign	Het
Ccr10	G	T	11: 101,174,666 (GRCm38)	L13I	probably benign	Het
Cfap52	A	G	11: 67,953,515 (GRCm38)	Y125H	probably damaging	Het
Cnr2	C	A	4: 135,917,625 (GRCm38)	T338K	possibly damaging	Het
Cntn2	T	A	1: 132,516,570 (GRCm38)	D935V	probably damaging	Het
Cog7	T	C	7: 121,943,844 (GRCm38)	K448R	possibly damaging	Het
Csnk1g2	G	A	10: 80,638,535 (GRCm38)	D197N	probably damaging	Het
Cyp2e1	T	A	7: 140,763,911 (GRCm38)	S21T	probably damaging	Het
Dcaf11	T	C	14: 55,564,135 (GRCm38)	F187L	probably damaging	Het
Dmd	T	A	X: 83,878,504 (GRCm38)	F1460Y	probably benign	Het
Dnah11	G	A	12: 117,911,040 (GRCm38)	A4030V	probably damaging	Het
Dnah7a	A	G	1: 53,522,360 (GRCm38)	V2046A	possibly damaging	Het
Dnajc6	T	C	4: 101,639,300 (GRCm38)	I820T	probably damaging	Het
Dsel	T	C	1: 111,860,732 (GRCm38)	D691G	possibly damaging	Het
Fbp1	T	A	13: 62,869,080 (GRCm38)	M203L	probably benign	Het
Fndc1	T	C	17: 7,773,638 (GRCm38)	T409A	unknown	Het
Golgb1	T	G	16: 36,925,849 (GRCm38)	L2930R	probably damaging	Het
Htr2a	A	G	14: 74,645,143 (GRCm38)	T190A	probably benign	Het
Klra4	C	T	6: 130,044,070 (GRCm38)	C254Y	probably damaging	Het
Large1	A	T	8: 73,132,039 (GRCm38)	V67E	probably benign	Het
Lins1	T	C	7: 66,714,183 (GRCm38)	S609P	probably damaging	Het
Magi3	T	C	3: 104,095,157 (GRCm38)	E156G	probably damaging	Het
Mdh1b	A	G	1: 63,715,364 (GRCm38)		probably benign	Het
Mfsd6	T	C	1: 52,708,878 (GRCm38)	D276G	probably benign	Het
Myh9	T	A	15: 77,796,020 (GRCm38)	K185*	probably null	Het
Myof	T	C	19: 37,920,779 (GRCm38)		probably null	Het
Naip2	T	G	13: 100,161,512 (GRCm38)	Y672S	possibly damaging	Het
Nbeal2	T	A	9: 110,628,276 (GRCm38)	H2273L	probably damaging	Het
Neb	T	C	2: 52,200,721 (GRCm38)	K1346E	possibly damaging	Het
Nfatc2	T	C	2: 168,504,450 (GRCm38)	D908G	probably damaging	Het
Nlgn2	T	C	11: 69,827,254 (GRCm38)	N375S	probably benign	Het
Nova1	G	T	12: 46,720,722 (GRCm38)	Q139K	unknown	Het
Olfr328	A	G	11: 58,552,161 (GRCm38)	L26P	probably damaging	Het
Olfr775	T	A	10: 129,250,925 (GRCm38)	Y130*	probably null	Het
Olfr978	T	A	9: 39,993,813 (GRCm38)	M1K	probably null	Het
Opa3	A	T	7: 19,228,582 (GRCm38)	Q47L	probably damaging	Het
Pacs1	A	T	19: 5,135,110 (GRCm38)		probably benign	Het
Pappa2	T	A	1: 158,782,259 (GRCm38)	H1544L	probably damaging	Het
Pax8	A	G	2: 24,444,615 (GRCm38)	S48P	probably damaging	Het
Pdilt	T	C	7: 119,498,049 (GRCm38)	N70S	possibly damaging	Het
Poldip3	T	C	15: 83,129,268 (GRCm38)		probably benign	Het
Ppp6r1	T	A	7: 4,642,212 (GRCm38)	I80F	probably damaging	Het
Pycr2	T	A	1: 180,904,739 (GRCm38)		probably null	Het
Rapgef2	C	T	3: 79,068,880 (GRCm38)		probably benign	Het
Rbm44	T	A	1: 91,153,180 (GRCm38)	D363E	probably damaging	Het
Rnf213	A	T	11: 119,427,510 (GRCm38)	I1046F	probably damaging	Het
Ryr2	A	G	13: 11,591,269 (GRCm38)	S4476P	probably damaging	Het
Scara5	G	A	14: 65,762,829 (GRCm38)	D483N	unknown	Het
Scmh1	T	A	4: 120,468,389 (GRCm38)	F101Y	probably damaging	Het
Sgo2a	T	A	1: 58,016,352 (GRCm38)	V565E	probably damaging	Het
Simc1	T	C	13: 54,525,258 (GRCm38)	M473T	probably benign	Het
Skint6	T	A	4: 113,238,184 (GRCm38)	R93*	probably null	Het
Skint7	T	C	4: 111,982,178 (GRCm38)	V223A	possibly damaging	Het
Slc25a2	T	C	18: 37,637,886 (GRCm38)	I197V	probably benign	Het
Slit2	A	G	5: 48,217,474 (GRCm38)	T361A	probably benign	Het
Sugp1	G	A	8: 70,070,126 (GRCm38)	G492D	probably damaging	Het
Svep1	C	T	4: 58,145,301 (GRCm38)	G388D	probably damaging	Het
Tbpl2	G	T	2: 24,093,876 (GRCm38)	A183E	probably damaging	Het
Tcerg1l	G	T	7: 138,229,890 (GRCm38)	P453T	probably damaging	Het
Tdpoz2	T	C	3: 93,651,739 (GRCm38)	T309A	probably benign	Het
Thbs4	T	A	13: 92,790,798 (GRCm38)	Y61F	probably benign	Het
Tmem117	C	A	15: 95,094,775 (GRCm38)	P439T	probably damaging	Het
Tmem151a	A	G	19: 5,082,965 (GRCm38)	V71A	probably benign	Het
Tmem268	G	T	4: 63,568,454 (GRCm38)		probably benign	Het
Tmem43	T	A	6: 91,477,374 (GRCm38)	Y48N	possibly damaging	Het
Tmigd1	T	C	11: 76,913,986 (GRCm38)	V217A	probably benign	Het
Tmprss11g	A	T	5: 86,497,329 (GRCm38)		probably benign	Het
Tsn	T	C	1: 118,309,821 (GRCm38)	I38V	probably benign	Het
Ttc41	A	T	10: 86,733,654 (GRCm38)	Y632F	probably damaging	Het
Vmn2r117	C	T	17: 23,475,578 (GRCm38)		probably benign	Het
Vmn2r12	A	T	5: 109,090,485 (GRCm38)	I463N	probably benign	Het
Wdsub1	T	A	2: 59,852,832 (GRCm38)	N466I	probably damaging	Het
Zdhhc21	A	T	4: 82,844,190 (GRCm38)	I56N	probably benign	Het
Zfand4	A	G	6: 116,273,656 (GRCm38)	T16A	possibly damaging	Het
Zmym4	T	C	4: 126,948,475 (GRCm38)	E15G	probably damaging	Het

Other mutations in Nbeal1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00094:Nbeal1	APN	1	60,235,191 (GRCm38)	nonsense	probably null	0.00
IGL00334:Nbeal1	APN	1	60,281,883 (GRCm38)	missense	probably damaging	0.98
IGL00334:Nbeal1	APN	1	60,328,103 (GRCm38)	missense	probably damaging	1.00
IGL00514:Nbeal1	APN	1	60,217,225 (GRCm38)	missense	probably benign	0.31
IGL00596:Nbeal1	APN	1	60,181,741 (GRCm38)	missense	probably damaging	0.96
IGL00654:Nbeal1	APN	1	60,195,011 (GRCm38)	critical splice acceptor site	probably benign	0.00
IGL00757:Nbeal1	APN	1	60,195,143 (GRCm38)	missense	possibly damaging	0.82
IGL00771:Nbeal1	APN	1	60,235,353 (GRCm38)	missense	probably benign	0.11
IGL01315:Nbeal1	APN	1	60,281,341 (GRCm38)	missense	probably damaging	1.00
IGL01445:Nbeal1	APN	1	60,242,625 (GRCm38)	critical splice donor site	probably null
IGL01456:Nbeal1	APN	1	60,230,628 (GRCm38)	missense	probably damaging	1.00
IGL01458:Nbeal1	APN	1	60,242,625 (GRCm38)	critical splice donor site	probably null
IGL01535:Nbeal1	APN	1	60,217,255 (GRCm38)	missense	probably damaging	1.00
IGL01608:Nbeal1	APN	1	60,242,535 (GRCm38)	critical splice acceptor site	probably benign	0.00
IGL02006:Nbeal1	APN	1	60,272,259 (GRCm38)	critical splice donor site	probably null
IGL02105:Nbeal1	APN	1	60,253,501 (GRCm38)	missense	probably damaging	1.00
IGL02409:Nbeal1	APN	1	60,329,335 (GRCm38)	missense	probably benign	0.01
IGL02713:Nbeal1	APN	1	60,235,237 (GRCm38)	missense	possibly damaging	0.94
IGL02720:Nbeal1	APN	1	60,283,987 (GRCm38)	missense	probably damaging	0.98
IGL02945:Nbeal1	APN	1	60,206,410 (GRCm38)	missense	probably damaging	1.00
IGL03023:Nbeal1	APN	1	60,253,413 (GRCm38)	missense	probably damaging	0.98
IGL03114:Nbeal1	APN	1	60,278,727 (GRCm38)	missense	probably damaging	1.00
IGL03231:Nbeal1	APN	1	60,236,459 (GRCm38)	missense	probably benign	0.44
IGL03241:Nbeal1	APN	1	60,234,868 (GRCm38)	missense	possibly damaging	0.46
IGL03241:Nbeal1	APN	1	60,234,869 (GRCm38)	missense	probably benign	0.44
IGL03382:Nbeal1	APN	1	60,261,586 (GRCm38)	critical splice donor site	probably null
IGL03412:Nbeal1	APN	1	60,242,567 (GRCm38)	nonsense	probably null
coach	UTSW	1	60,253,481 (GRCm38)	nonsense	probably null
Committee	UTSW	1	60,292,903 (GRCm38)	missense	probably damaging	1.00
Disgrace	UTSW	1	60,281,310 (GRCm38)	nonsense	probably null
Dravrah	UTSW	1	60,284,092 (GRCm38)	missense	probably damaging	1.00
Harvard	UTSW	1	60,235,563 (GRCm38)	splice site	probably null
horrified	UTSW	1	60,244,824 (GRCm38)	missense	probably damaging	1.00
Lampoon	UTSW	1	60,261,586 (GRCm38)	critical splice donor site	probably null
lawyer	UTSW	1	60,310,224 (GRCm38)	nonsense	probably null
magistrate	UTSW	1	60,194,597 (GRCm38)	critical splice donor site	probably null
Maratimus	UTSW	1	60,291,888 (GRCm38)	missense	probably damaging	1.00
National	UTSW	1	60,222,263 (GRCm38)	missense	possibly damaging	0.95
phainopepla	UTSW	1	60,319,687 (GRCm38)	missense	probably damaging	1.00
R3875_Nbeal1_770	UTSW	1	60,194,599 (GRCm38)	splice site	probably benign
satirical	UTSW	1	60,235,562 (GRCm38)	critical splice donor site	probably null
silky	UTSW	1	60,330,878 (GRCm38)	splice site	probably benign
stiggs	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
3-1:Nbeal1	UTSW	1	60,264,272 (GRCm38)	splice site	probably benign
P0007:Nbeal1	UTSW	1	60,319,688 (GRCm38)	missense	probably damaging	0.98
P0028:Nbeal1	UTSW	1	60,291,937 (GRCm38)	missense	probably damaging	1.00
R0041:Nbeal1	UTSW	1	60,281,871 (GRCm38)	missense	probably benign	0.05
R0051:Nbeal1	UTSW	1	60,310,263 (GRCm38)	missense	probably benign	0.19
R0052:Nbeal1	UTSW	1	60,228,612 (GRCm38)	splice site	probably benign
R0054:Nbeal1	UTSW	1	60,287,401 (GRCm38)	utr 3 prime	probably benign
R0062:Nbeal1	UTSW	1	60,247,717 (GRCm38)	missense	probably benign	0.01
R0062:Nbeal1	UTSW	1	60,247,717 (GRCm38)	missense	probably benign	0.01
R0094:Nbeal1	UTSW	1	60,305,309 (GRCm38)	missense	possibly damaging	0.62
R0310:Nbeal1	UTSW	1	60,305,370 (GRCm38)	splice site	probably benign
R0324:Nbeal1	UTSW	1	60,292,873 (GRCm38)	missense	probably damaging	1.00
R0329:Nbeal1	UTSW	1	60,268,063 (GRCm38)	missense	probably damaging	1.00
R0330:Nbeal1	UTSW	1	60,268,063 (GRCm38)	missense	probably damaging	1.00
R0417:Nbeal1	UTSW	1	60,247,734 (GRCm38)	missense	probably benign	0.00
R0421:Nbeal1	UTSW	1	60,268,439 (GRCm38)	missense	probably benign	0.08
R0617:Nbeal1	UTSW	1	60,281,832 (GRCm38)	nonsense	probably null
R1034:Nbeal1	UTSW	1	60,290,006 (GRCm38)	nonsense	probably null
R1082:Nbeal1	UTSW	1	60,312,226 (GRCm38)	missense	probably damaging	0.99
R1123:Nbeal1	UTSW	1	60,260,269 (GRCm38)	missense	probably benign
R1187:Nbeal1	UTSW	1	60,194,528 (GRCm38)	missense	probably damaging	1.00
R1484:Nbeal1	UTSW	1	60,200,939 (GRCm38)	missense	probably damaging	1.00
R1594:Nbeal1	UTSW	1	60,305,291 (GRCm38)	missense	possibly damaging	0.91
R1651:Nbeal1	UTSW	1	60,200,119 (GRCm38)	missense	probably damaging	1.00
R1678:Nbeal1	UTSW	1	60,260,334 (GRCm38)	missense	probably benign	0.00
R1806:Nbeal1	UTSW	1	60,284,092 (GRCm38)	missense	probably damaging	1.00
R1937:Nbeal1	UTSW	1	60,267,941 (GRCm38)	nonsense	probably null
R1952:Nbeal1	UTSW	1	60,234,840 (GRCm38)	missense	probably damaging	1.00
R1953:Nbeal1	UTSW	1	60,234,840 (GRCm38)	missense	probably damaging	1.00
R2038:Nbeal1	UTSW	1	60,206,344 (GRCm38)	missense	probably benign	0.00
R2044:Nbeal1	UTSW	1	60,319,687 (GRCm38)	missense	probably damaging	1.00
R2050:Nbeal1	UTSW	1	60,292,964 (GRCm38)	splice site	probably null
R2055:Nbeal1	UTSW	1	60,311,057 (GRCm38)	missense	probably damaging	1.00
R2064:Nbeal1	UTSW	1	60,270,356 (GRCm38)	missense	possibly damaging	0.89
R2100:Nbeal1	UTSW	1	60,305,271 (GRCm38)	splice site	probably null
R2181:Nbeal1	UTSW	1	60,278,780 (GRCm38)	missense	probably damaging	1.00
R2192:Nbeal1	UTSW	1	60,281,895 (GRCm38)	missense	probably damaging	1.00
R2203:Nbeal1	UTSW	1	60,284,006 (GRCm38)	missense	probably benign	0.21
R2267:Nbeal1	UTSW	1	60,330,878 (GRCm38)	splice site	probably benign
R2268:Nbeal1	UTSW	1	60,330,878 (GRCm38)	splice site	probably benign
R2351:Nbeal1	UTSW	1	60,237,098 (GRCm38)	missense	possibly damaging	0.90
R2366:Nbeal1	UTSW	1	60,251,352 (GRCm38)	missense	probably damaging	0.97
R2393:Nbeal1	UTSW	1	60,251,370 (GRCm38)	missense	probably damaging	0.98
R3545:Nbeal1	UTSW	1	60,278,780 (GRCm38)	missense	probably damaging	1.00
R3546:Nbeal1	UTSW	1	60,278,780 (GRCm38)	missense	probably damaging	1.00
R3547:Nbeal1	UTSW	1	60,278,780 (GRCm38)	missense	probably damaging	1.00
R3701:Nbeal1	UTSW	1	60,251,413 (GRCm38)	splice site	probably benign
R3747:Nbeal1	UTSW	1	60,195,023 (GRCm38)	missense	probably damaging	0.98
R3875:Nbeal1	UTSW	1	60,194,599 (GRCm38)	splice site	probably benign
R4119:Nbeal1	UTSW	1	60,291,870 (GRCm38)	missense	probably damaging	0.99
R4256:Nbeal1	UTSW	1	60,330,948 (GRCm38)	missense	probably benign	0.19
R4371:Nbeal1	UTSW	1	60,289,946 (GRCm38)	missense	possibly damaging	0.95
R4450:Nbeal1	UTSW	1	60,267,774 (GRCm38)	missense	probably damaging	0.97
R4558:Nbeal1	UTSW	1	60,281,310 (GRCm38)	nonsense	probably null
R4618:Nbeal1	UTSW	1	60,228,731 (GRCm38)	intron	probably benign
R4673:Nbeal1	UTSW	1	60,329,390 (GRCm38)	missense	probably damaging	1.00
R4719:Nbeal1	UTSW	1	60,235,563 (GRCm38)	splice site	probably null
R4798:Nbeal1	UTSW	1	60,222,193 (GRCm38)	splice site	probably null
R4826:Nbeal1	UTSW	1	60,251,342 (GRCm38)	missense	possibly damaging	0.79
R4841:Nbeal1	UTSW	1	60,253,375 (GRCm38)	missense	probably damaging	1.00
R4842:Nbeal1	UTSW	1	60,253,375 (GRCm38)	missense	probably damaging	1.00
R4895:Nbeal1	UTSW	1	60,292,903 (GRCm38)	missense	probably damaging	1.00
R4929:Nbeal1	UTSW	1	60,238,654 (GRCm38)	missense	probably damaging	1.00
R5026:Nbeal1	UTSW	1	60,237,179 (GRCm38)	missense	probably damaging	1.00
R5243:Nbeal1	UTSW	1	60,270,328 (GRCm38)	missense	probably damaging	0.99
R5300:Nbeal1	UTSW	1	60,235,559 (GRCm38)	nonsense	probably null
R5345:Nbeal1	UTSW	1	60,328,210 (GRCm38)	critical splice donor site	probably null
R5502:Nbeal1	UTSW	1	60,310,999 (GRCm38)	missense	probably damaging	1.00
R5542:Nbeal1	UTSW	1	60,277,194 (GRCm38)	missense	probably benign	0.00
R5555:Nbeal1	UTSW	1	60,237,152 (GRCm38)	missense	possibly damaging	0.93
R5580:Nbeal1	UTSW	1	60,242,602 (GRCm38)	missense	probably benign	0.45
R5765:Nbeal1	UTSW	1	60,291,847 (GRCm38)	missense	probably damaging	1.00
R5802:Nbeal1	UTSW	1	60,272,221 (GRCm38)	missense	probably benign	0.01
R5907:Nbeal1	UTSW	1	60,228,791 (GRCm38)	intron	probably benign
R5918:Nbeal1	UTSW	1	60,267,892 (GRCm38)	missense	possibly damaging	0.90
R5923:Nbeal1	UTSW	1	60,248,395 (GRCm38)	missense	probably damaging	1.00
R6066:Nbeal1	UTSW	1	60,248,405 (GRCm38)	missense	probably benign	0.29
R6091:Nbeal1	UTSW	1	60,181,556 (GRCm38)	start gained	probably benign
R6113:Nbeal1	UTSW	1	60,222,263 (GRCm38)	missense	possibly damaging	0.95
R6143:Nbeal1	UTSW	1	60,251,307 (GRCm38)	missense	possibly damaging	0.81
R6194:Nbeal1	UTSW	1	60,257,484 (GRCm38)	missense	possibly damaging	0.80
R6197:Nbeal1	UTSW	1	60,222,128 (GRCm38)	missense	probably damaging	0.99
R6228:Nbeal1	UTSW	1	60,295,924 (GRCm38)	missense	probably benign	0.00
R6229:Nbeal1	UTSW	1	60,248,365 (GRCm38)	missense	possibly damaging	0.88
R6309:Nbeal1	UTSW	1	60,238,719 (GRCm38)	missense	probably benign
R6457:Nbeal1	UTSW	1	60,253,474 (GRCm38)	missense	probably benign	0.31
R6489:Nbeal1	UTSW	1	60,330,942 (GRCm38)	missense	possibly damaging	0.89
R6845:Nbeal1	UTSW	1	60,281,310 (GRCm38)	nonsense	probably null
R7021:Nbeal1	UTSW	1	60,261,586 (GRCm38)	critical splice donor site	probably null
R7033:Nbeal1	UTSW	1	60,310,947 (GRCm38)	missense	probably damaging	1.00
R7144:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7145:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7146:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7157:Nbeal1	UTSW	1	60,260,634 (GRCm38)	nonsense	probably null
R7157:Nbeal1	UTSW	1	60,237,158 (GRCm38)	missense	probably damaging	1.00
R7209:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7210:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7211:Nbeal1	UTSW	1	60,200,951 (GRCm38)	missense	probably damaging	1.00
R7212:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7213:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7214:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7283:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7285:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7287:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7296:Nbeal1	UTSW	1	60,310,224 (GRCm38)	nonsense	probably null
R7312:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7313:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7329:Nbeal1	UTSW	1	60,217,196 (GRCm38)	missense	probably benign	0.39
R7380:Nbeal1	UTSW	1	60,244,810 (GRCm38)	missense	probably damaging	1.00
R7414:Nbeal1	UTSW	1	60,194,597 (GRCm38)	critical splice donor site	probably null
R7477:Nbeal1	UTSW	1	60,261,584 (GRCm38)	missense	probably benign
R7507:Nbeal1	UTSW	1	60,235,467 (GRCm38)	missense	probably damaging	1.00
R7642:Nbeal1	UTSW	1	60,277,227 (GRCm38)	missense	probably benign	0.31
R7678:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7689:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7728:Nbeal1	UTSW	1	60,244,824 (GRCm38)	missense	probably damaging	1.00
R7757:Nbeal1	UTSW	1	60,257,450 (GRCm38)	missense	probably damaging	0.97
R7761:Nbeal1	UTSW	1	60,319,341 (GRCm38)	missense	probably benign	0.00
R7813:Nbeal1	UTSW	1	60,291,889 (GRCm38)	missense	probably damaging	1.00
R7829:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R7891:Nbeal1	UTSW	1	60,260,432 (GRCm38)	missense	probably benign
R7902:Nbeal1	UTSW	1	60,291,870 (GRCm38)	missense	probably damaging	0.99
R8022:Nbeal1	UTSW	1	60,260,272 (GRCm38)	nonsense	probably null
R8053:Nbeal1	UTSW	1	60,279,795 (GRCm38)	missense	probably damaging	0.98
R8169:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R8170:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R8178:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R8182:Nbeal1	UTSW	1	60,200,133 (GRCm38)	missense	probably benign	0.00
R8186:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R8187:Nbeal1	UTSW	1	60,237,151 (GRCm38)	missense	probably benign	0.11
R8193:Nbeal1	UTSW	1	60,253,481 (GRCm38)	nonsense	probably null
R8209:Nbeal1	UTSW	1	60,277,177 (GRCm38)	missense	probably damaging	0.99
R8226:Nbeal1	UTSW	1	60,277,177 (GRCm38)	missense	probably damaging	0.99
R8549:Nbeal1	UTSW	1	60,235,562 (GRCm38)	critical splice donor site	probably null
R8560:Nbeal1	UTSW	1	60,235,157 (GRCm38)	missense	probably benign	0.38
R8753:Nbeal1	UTSW	1	60,268,383 (GRCm38)	missense	probably damaging	1.00
R8769:Nbeal1	UTSW	1	60,235,211 (GRCm38)	missense	probably damaging	0.99
R8771:Nbeal1	UTSW	1	60,261,584 (GRCm38)	missense	probably benign
R8952:Nbeal1	UTSW	1	60,260,300 (GRCm38)	missense	probably benign	0.01
R9014:Nbeal1	UTSW	1	60,289,959 (GRCm38)	missense	probably damaging	1.00
R9056:Nbeal1	UTSW	1	60,278,726 (GRCm38)	missense	probably damaging	1.00
R9091:Nbeal1	UTSW	1	60,268,389 (GRCm38)	missense	possibly damaging	0.50
R9138:Nbeal1	UTSW	1	60,247,745 (GRCm38)	nonsense	probably null
R9168:Nbeal1	UTSW	1	60,291,888 (GRCm38)	missense	probably damaging	1.00
R9200:Nbeal1	UTSW	1	60,281,266 (GRCm38)	missense	probably damaging	1.00
R9205:Nbeal1	UTSW	1	60,278,680 (GRCm38)	missense	probably damaging	1.00
R9270:Nbeal1	UTSW	1	60,268,389 (GRCm38)	missense	possibly damaging	0.50
R9322:Nbeal1	UTSW	1	60,258,659 (GRCm38)	missense	possibly damaging	0.91
R9405:Nbeal1	UTSW	1	60,310,265 (GRCm38)	missense	probably damaging	1.00
R9554:Nbeal1	UTSW	1	60,251,128 (GRCm38)	nonsense	probably null
R9557:Nbeal1	UTSW	1	60,235,350 (GRCm38)	missense	probably benign
R9560:Nbeal1	UTSW	1	60,329,385 (GRCm38)	missense	probably damaging	1.00
R9641:Nbeal1	UTSW	1	60,311,088 (GRCm38)	missense	probably damaging	1.00
R9784:Nbeal1	UTSW	1	60,260,582 (GRCm38)	nonsense	probably null
X0022:Nbeal1	UTSW	1	60,277,232 (GRCm38)	missense	probably benign

Posted On

2015-12-18