Mutagenetix > Incidental Mutation

Incidental Mutation 'R4732:Ahnak'

359122

Institutional Source

Beutler Lab

Gene Symbol

Ahnak

Ensembl Gene

ENSMUSG00000069833

Gene Name

AHNAK nucleoprotein (desmoyokin)

Synonyms

1110004P15Rik, 2310047C17Rik, DY6

MMRRC Submission

042022-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.368) question?

Stock #

R4732 (G1)

Quality Score

129

Status

Validated

Chromosome

Chromosomal Location

8989284-9076919 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 9007301 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Valine at position 1983 (G1983V)

Ref Sequence

ENSEMBL: ENSMUSP00000090633 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092955] [ENSMUST00000092956]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000092955

SMART Domains

Protein: ENSMUSP00000090632
Gene: ENSMUSG00000069833

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
PDZ	20	91	2.31e-5	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000092956
AA Change: G1983V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000090633
Gene: ENSMUSG00000069833
AA Change: G1983V

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
PDZ	20	91	2.31e-5	SMART
internal_repeat_2	163	1515	5.22e-182	PROSPERO
internal_repeat_1	224	2314	N/A	PROSPERO
internal_repeat_2	1532	3028	5.22e-182	PROSPERO
internal_repeat_1	2660	5095	N/A	PROSPERO
low complexity region	5336	5353	N/A	INTRINSIC
low complexity region	5493	5504	N/A	INTRINSIC
low complexity region	5580	5600	N/A	INTRINSIC
low complexity region	5620	5636	N/A	INTRINSIC

Meta Mutation Damage Score

0.1268

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 95.1%

Validation Efficiency

99% (110/111)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a large (700 kDa) structural scaffold protein consisting of a central domain with 128 aa repeats. The encoded protein may play a role in such diverse processes as blood-brain barrier formation, cell structure and migration, cardiac calcium channel regulation, and tumor metastasis. A much shorter variant encoding a 17 kDa isoform exists for this gene, and the shorter isoform initiates a feedback loop that regulates alternative splicing of this gene. [provided by RefSeq, Oct 2016]
PHENOTYPE: Mice homozygous for one knock-out allele exhibit decreased T cell proliferation and increased susceptibility to parasitic infection. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 192 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700128F08Rik	T	A	9: 8,222,173 (GRCm38)		noncoding transcript	Het
3110035E14Rik	T	C	1: 9,606,976 (GRCm38)	S24P	probably benign	Het
4933409G03Rik	A	G	2: 68,614,721 (GRCm38)		probably benign	Het
Acan	T	C	7: 79,098,609 (GRCm38)	S1043P	probably damaging	Het
Ackr2	A	G	9: 121,909,183 (GRCm38)	Y208C	probably damaging	Het
Actg1	C	T	11: 120,347,479 (GRCm38)		probably benign	Het
Adam1a	T	A	5: 121,519,434 (GRCm38)	T599S	probably benign	Het
Adamts12	A	T	15: 11,270,662 (GRCm38)	S668C	probably damaging	Het
Adcy8	A	G	15: 64,754,862 (GRCm38)	V709A	possibly damaging	Het
Adgrf2	A	C	17: 42,710,754 (GRCm38)	I393S	probably damaging	Het
AI413582	A	G	17: 27,565,270 (GRCm38)		probably benign	Het
Aim2	T	A	1: 173,463,876 (GRCm38)	D282E	possibly damaging	Het
Ak8	A	G	2: 28,760,071 (GRCm38)	Y370C	probably damaging	Het
Akap9	A	G	5: 4,013,901 (GRCm38)	D1750G	probably damaging	Het
Als2cl	T	A	9: 110,889,136 (GRCm38)	V315E	probably damaging	Het
Ankrd28	A	C	14: 31,755,741 (GRCm38)	C115G	probably benign	Het
Ap3b2	C	T	7: 81,471,932 (GRCm38)	A519T	probably damaging	Het
Apool	C	T	X: 112,372,200 (GRCm38)	T166I	probably damaging	Het
Arhgef2	A	T	3: 88,631,940 (GRCm38)	K65*	probably null	Het
Arhgef38	G	T	3: 133,132,269 (GRCm38)	Y633*	probably null	Het
Asah2	T	C	19: 31,995,358 (GRCm38)	N659S	probably benign	Het
Atf7ip2	A	G	16: 10,241,886 (GRCm38)	D430G	possibly damaging	Het
Atp8a1	G	A	5: 67,813,120 (GRCm38)	S92L	probably benign	Het
Bag4	C	T	8: 25,769,488 (GRCm38)	A228T	probably benign	Het
BC024978	T	A	7: 27,201,043 (GRCm38)	M149K	probably damaging	Het
C130073F10Rik	C	A	4: 101,890,710 (GRCm38)	S89I	probably benign	Het
Cacna1g	T	C	11: 94,443,215 (GRCm38)	T867A	probably damaging	Het
Ccdc88a	T	G	11: 29,485,906 (GRCm38)	N1276K	probably benign	Het
Cdc42bpg	T	A	19: 6,311,191 (GRCm38)	V282E	probably damaging	Het
Cdipt	T	A	7: 126,978,358 (GRCm38)	L92H	probably damaging	Het
Celsr2	T	A	3: 108,398,952 (GRCm38)	D2012V	probably damaging	Het
Cenpt	A	G	8: 105,847,136 (GRCm38)	V254A	probably benign	Het
Cep104	T	A	4: 153,988,426 (GRCm38)	D380E	probably damaging	Het
Cers5	C	T	15: 99,741,637 (GRCm38)	R123Q	probably benign	Het
Ces2h	A	G	8: 105,014,604 (GRCm38)	E76G	probably damaging	Het
Cfap77	T	A	2: 28,984,388 (GRCm38)	E143D	probably benign	Het
Chmp7	C	A	14: 69,732,296 (GRCm38)	R65L	probably damaging	Het
Cldnd2	T	A	7: 43,442,189 (GRCm38)	C65S	possibly damaging	Het
Clec2g	C	A	6: 128,981,879 (GRCm38)	Y142*	probably null	Het
Coch	A	T	12: 51,605,019 (GRCm38)	E549V	probably benign	Het
Cog7	T	C	7: 121,964,244 (GRCm38)	D215G	probably benign	Het
Col4a2	A	G	8: 11,446,197 (GRCm38)	H1606R	probably benign	Het
Col4a2	T	C	8: 11,414,779 (GRCm38)	V348A	probably benign	Het
Cpd	T	C	11: 76,811,794 (GRCm38)	N583D	probably damaging	Het
Cyp2d11	T	A	15: 82,389,227 (GRCm38)	Y481F	probably benign	Het
D130043K22Rik	T	C	13: 24,899,665 (GRCm38)	S1038P	probably damaging	Het
Deptor	C	A	15: 55,181,010 (GRCm38)	H191N	probably benign	Het
Dgkz	A	T	2: 91,938,339 (GRCm38)	I699N	probably damaging	Het
Dnah12	C	T	14: 26,781,784 (GRCm38)	T1653I	probably damaging	Het
Dnah7c	T	A	1: 46,770,173 (GRCm38)	N3550K	probably damaging	Het
Dnah8	A	G	17: 30,775,061 (GRCm38)	K3384R	probably null	Het
Dnajc11	A	G	4: 151,970,967 (GRCm38)		probably benign	Het
Dnajc13	CT	C	9: 104,186,805 (GRCm38)		probably benign	Het
Dnhd1	C	A	7: 105,673,849 (GRCm38)	N521K	probably benign	Het
Drg2	T	C	11: 60,461,396 (GRCm38)		probably null	Het
Dync1h1	C	T	12: 110,649,507 (GRCm38)	Q3030*	probably null	Het
Efhb	G	A	17: 53,426,244 (GRCm38)	T533I	probably damaging	Het
Eif2d	T	C	1: 131,164,727 (GRCm38)	V374A	probably damaging	Het
Etfb	T	C	7: 43,444,200 (GRCm38)	V17A	probably damaging	Het
F5	C	T	1: 164,181,657 (GRCm38)	T332M	probably damaging	Het
Fcho1	T	C	8: 71,716,795 (GRCm38)	T156A	probably benign	Het
Fn1	A	T	1: 71,602,512 (GRCm38)		probably null	Het
Fnip2	A	T	3: 79,481,652 (GRCm38)	S561T	probably damaging	Het
Frs2	T	A	10: 117,074,093 (GRCm38)	T455S	probably benign	Het
Fry	G	A	5: 150,386,007 (GRCm38)	E639K		Het
Fto	T	A	8: 91,409,714 (GRCm38)	D205E	probably damaging	Het
Galntl6	G	A	8: 58,427,813 (GRCm38)	P147L	probably damaging	Het
Gigyf1	T	A	5: 137,524,770 (GRCm38)	D844E	probably benign	Het
Gle1	T	C	2: 29,940,232 (GRCm38)	S267P	probably damaging	Het
Glg1	G	A	8: 111,187,755 (GRCm38)	R466W	probably damaging	Het
Gm10277	T	C	11: 77,786,097 (GRCm38)		probably benign	Het
Gm20388	A	G	8: 122,270,274 (GRCm38)		probably benign	Het
Gm5724	A	T	6: 141,723,179 (GRCm38)	M509K	probably benign	Het
Gm6871	T	C	7: 41,546,749 (GRCm38)	I39V	probably benign	Het
Gm9970	A	G	5: 31,241,066 (GRCm38)		probably benign	Het
Gpr35	T	G	1: 92,983,385 (GRCm38)	I57S	probably damaging	Het
Gprin1	C	T	13: 54,739,957 (GRCm38)	G168E	possibly damaging	Het
Gtdc1	A	G	2: 44,789,055 (GRCm38)		probably benign	Het
Gtf3c2	G	T	5: 31,160,057 (GRCm38)	P586T	probably damaging	Het
Gucy1a2	A	T	9: 3,759,424 (GRCm38)	H410L	probably benign	Het
Gucy2c	A	G	6: 136,767,152 (GRCm38)	S150P	probably damaging	Het
Ifi214	T	C	1: 173,526,591 (GRCm38)	Q171R	probably benign	Het
Ifit1bl1	T	C	19: 34,594,321 (GRCm38)	I245M	probably benign	Het
Igkv4-50	T	C	6: 69,701,000 (GRCm38)	K40R	probably benign	Het
Igkv8-18	T	A	6: 70,356,296 (GRCm38)	I74N	probably damaging	Het
Il2ra	T	A	2: 11,676,920 (GRCm38)	M112K	probably benign	Het
Itpr2	A	G	6: 146,373,173 (GRCm38)	F837S	probably damaging	Het
Kbtbd7	T	C	14: 79,428,800 (GRCm38)	*691Q	probably null	Het
Kcnn2	T	A	18: 45,560,349 (GRCm38)	S331T	possibly damaging	Het
Khnyn	T	A	14: 55,886,489 (GRCm38)		probably null	Het
Kif26a	G	A	12: 112,175,573 (GRCm38)	A754T	probably benign	Het
Klra3	T	A	6: 130,327,132 (GRCm38)	Y199F	possibly damaging	Het
Lhx2	A	G	2: 38,359,991 (GRCm38)	K274R	probably damaging	Het
Lrp2	T	C	2: 69,533,555 (GRCm38)	I313V	probably benign	Het
Lrrfip1	A	T	1: 91,115,647 (GRCm38)	E591D	probably benign	Het
Lrrk2	A	C	15: 91,688,849 (GRCm38)	E200A	probably damaging	Het
Lrrk2	G	A	15: 91,765,747 (GRCm38)	E1696K	probably damaging	Het
Mast4	A	T	13: 102,772,572 (GRCm38)	M465K	probably damaging	Het
Moxd2	T	G	6: 40,878,859 (GRCm38)	I599L	probably benign	Het
Mug2	T	C	6: 122,071,872 (GRCm38)	S866P	probably damaging	Het
Ncam2	A	G	16: 81,434,884 (GRCm38)	T79A	possibly damaging	Het
Ncoa6	C	A	2: 155,421,301 (GRCm38)	Q404H	probably damaging	Het
Neb	A	G	2: 52,279,079 (GRCm38)	Y1815H	probably damaging	Het
Nell1	A	G	7: 50,856,217 (GRCm38)	D724G	probably damaging	Het
Nkx3-2	A	G	5: 41,762,144 (GRCm38)	V167A	probably benign	Het
Nsun3	C	A	16: 62,735,119 (GRCm38)	C348F	possibly damaging	Het
Obox6	A	T	7: 15,834,772 (GRCm38)	S60T	possibly damaging	Het
Olfr1	T	C	11: 73,395,695 (GRCm38)	D109G	probably benign	Het
Olfr1378	G	A	11: 50,969,266 (GRCm38)	V83M	possibly damaging	Het
Olfr138	T	A	17: 38,275,547 (GRCm38)	Y259N	probably damaging	Het
Olfr466	T	C	13: 65,152,653 (GRCm38)	V143A	possibly damaging	Het
Olfr744	T	A	14: 50,618,569 (GRCm38)	C116S	probably benign	Het
Olfr94	T	C	17: 37,197,024 (GRCm38)	T315A	probably damaging	Het
Olfr980	A	T	9: 40,006,268 (GRCm38)	I227N	probably damaging	Het
Oog2	T	A	4: 144,193,941 (GRCm38)		probably benign	Het
Pabpc1	A	T	15: 36,599,284 (GRCm38)	V389E	probably benign	Het
Pank4	A	T	4: 154,971,390 (GRCm38)	M291L	probably benign	Het
Pcf11	T	C	7: 92,658,833 (GRCm38)	D709G	probably benign	Het
Pcgf1	T	A	6: 83,079,957 (GRCm38)		probably benign	Het
Pcnx	A	G	12: 81,995,751 (GRCm38)	I2256V	probably benign	Het
Pex6	A	G	17: 46,724,707 (GRCm38)		probably null	Het
Pex6	A	G	17: 46,722,288 (GRCm38)	D579G	probably benign	Het
Piezo2	C	T	18: 63,030,401 (GRCm38)	A2149T	probably damaging	Het
Pik3c2g	A	G	6: 139,935,985 (GRCm38)	E781G	probably benign	Het
Pik3r4	G	A	9: 105,678,176 (GRCm38)	V1111I	possibly damaging	Het
Pkd1l2	T	A	8: 116,995,842 (GRCm38)		probably null	Het
Plekhg1	T	A	10: 3,957,506 (GRCm38)	S808T	probably benign	Het
Pnkp	T	A	7: 44,860,454 (GRCm38)		probably benign	Het
Polr3c	A	T	3: 96,723,661 (GRCm38)	F148I	probably damaging	Het
Ppard	A	T	17: 28,286,443 (GRCm38)	T35S	probably benign	Het
Ptov1	T	C	7: 44,867,109 (GRCm38)	D134G	probably benign	Het
Ptprz1	T	A	6: 23,002,610 (GRCm38)	S1566R	probably benign	Het
Pum1	T	C	4: 130,718,193 (GRCm38)	S158P	probably benign	Het
Qk	T	C	17: 10,216,288 (GRCm38)	H269R	probably damaging	Het
Qrsl1	T	C	10: 43,876,663 (GRCm38)	Y388C	probably damaging	Het
Rapgef1	T	G	2: 29,689,160 (GRCm38)	I182S	probably damaging	Het
Ret	T	C	6: 118,163,193 (GRCm38)	S1013G	possibly damaging	Het
Rimbp3	A	G	16: 17,210,601 (GRCm38)	R630G	possibly damaging	Het
Rnmt	A	T	18: 68,317,960 (GRCm38)		probably benign	Het
Ryr2	A	T	13: 11,577,909 (GRCm38)	M4653K	possibly damaging	Het
Sacm1l	G	A	9: 123,590,830 (GRCm38)	V553I	probably benign	Het
Sec31b	A	T	19: 44,532,677 (GRCm38)	S110T	probably damaging	Het
Serpina3k	G	A	12: 104,340,860 (GRCm38)	G117D	probably damaging	Het
Sesn2	T	C	4: 132,494,591 (GRCm38)	Y410C	probably damaging	Het
Slc24a1	G	A	9: 64,949,554 (GRCm38)	R24C	probably benign	Het
Slc35g2	A	C	9: 100,552,502 (GRCm38)	V372G	probably benign	Het
Slc7a7	T	C	14: 54,408,733 (GRCm38)	Y91C	probably damaging	Het
Slc7a9	T	A	7: 35,453,563 (GRCm38)	Y135*	probably null	Het
Slco4a1	A	G	2: 180,473,615 (GRCm38)	N662D	probably damaging	Het
Slfn4	T	A	11: 83,189,282 (GRCm38)		probably benign	Het
Slmap	T	C	14: 26,468,535 (GRCm38)	N156S	probably damaging	Het
Snx18	A	G	13: 113,617,774 (GRCm38)	S208P	probably benign	Het
Sorbs1	T	A	19: 40,314,689 (GRCm38)	R485S	probably benign	Het
Spib	A	G	7: 44,528,885 (GRCm38)	S154P	probably damaging	Het
Spty2d1	T	C	7: 46,996,110 (GRCm38)	D595G	probably damaging	Het
St7	T	A	6: 17,906,516 (GRCm38)		probably null	Het
Susd1	T	C	4: 59,428,029 (GRCm38)	T52A	possibly damaging	Het
Svs2	T	A	2: 164,237,123 (GRCm38)	D288V	possibly damaging	Het
Syt7	T	A	19: 10,442,924 (GRCm38)	I355N	probably damaging	Het
Tarm1	G	A	7: 3,496,900 (GRCm38)	Q145*	probably null	Het
Teddm2	T	A	1: 153,850,741 (GRCm38)	E76V	probably damaging	Het
Thsd7b	T	C	1: 129,613,186 (GRCm38)	S343P	probably damaging	Het
Tigd2	T	A	6: 59,211,415 (GRCm38)	H422Q	probably benign	Het
Tle1	T	C	4: 72,125,019 (GRCm38)	N538D	possibly damaging	Het
Tmc2	A	G	2: 130,261,397 (GRCm38)		probably null	Het
Tmtc1	A	C	6: 148,284,980 (GRCm38)		probably null	Het
Tns3	C	T	11: 8,450,986 (GRCm38)	R1104H	probably benign	Het
Trim6	T	C	7: 104,232,648 (GRCm38)	Y369H	probably damaging	Het
Triobp	G	A	15: 78,967,113 (GRCm38)	R489K	probably damaging	Het
Trpv4	T	C	5: 114,622,753 (GRCm38)	D732G	possibly damaging	Het
Trrap	G	A	5: 144,816,570 (GRCm38)	V1883I	probably damaging	Het
Tsc2	C	A	17: 24,603,275 (GRCm38)	V1141F	possibly damaging	Het
Ttn	A	T	2: 76,943,011 (GRCm38)	M2395K	unknown	Het
Ttn	A	G	2: 76,899,827 (GRCm38)		probably benign	Het
Tyrp1	A	T	4: 80,844,935 (GRCm38)	D353V	possibly damaging	Het
Ubd	A	C	17: 37,195,702 (GRCm38)	T160P	probably benign	Het
Ugt2b36	G	T	5: 87,081,538 (GRCm38)	Y156*	probably null	Het
Ulk4	G	A	9: 121,263,638 (GRCm38)	R178*	probably null	Het
Unc13d	A	G	11: 116,073,582 (GRCm38)	V312A	possibly damaging	Het
Urb2	G	T	8: 124,028,897 (GRCm38)	A448S	probably damaging	Het
Urod	G	A	4: 116,991,673 (GRCm38)	A92V	possibly damaging	Het
Vmn1r33	T	A	6: 66,611,819 (GRCm38)	R250S	probably benign	Het
Vmn1r87	A	T	7: 13,132,327 (GRCm38)	M11K	possibly damaging	Het
Vmn2r77	C	T	7: 86,800,987 (GRCm38)	T147I	probably benign	Het
Vstm4	A	G	14: 32,917,902 (GRCm38)	K96E	possibly damaging	Het
Washc4	A	T	10: 83,574,479 (GRCm38)	M644L	probably benign	Het
Wwp1	T	C	4: 19,661,990 (GRCm38)	D172G	probably benign	Het
Zbtb38	A	T	9: 96,687,684 (GRCm38)	V449E	probably damaging	Het
Zfhx4	T	C	3: 5,214,807 (GRCm38)		probably benign	Het
Zfp229	C	T	17: 21,745,286 (GRCm38)	H166Y	possibly damaging	Het
Zfp512b	A	G	2: 181,588,739 (GRCm38)	S453P	probably benign	Het
Zp2	C	A	7: 120,138,120 (GRCm38)	V282L	probably damaging	Het

Other mutations in Ahnak

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00467:Ahnak	APN	19	9,007,223 (GRCm38)	missense	probably damaging	0.99
IGL00509:Ahnak	APN	19	9,009,951 (GRCm38)	missense	possibly damaging	0.94
IGL00539:Ahnak	APN	19	9,007,908 (GRCm38)	missense	possibly damaging	0.50
IGL00558:Ahnak	APN	19	9,004,307 (GRCm38)	missense	possibly damaging	0.93
IGL00567:Ahnak	APN	19	9,013,383 (GRCm38)	missense	probably benign	0.24
IGL00706:Ahnak	APN	19	9,013,730 (GRCm38)	nonsense	probably null
IGL00807:Ahnak	APN	19	9,008,522 (GRCm38)	missense	possibly damaging	0.92
IGL00870:Ahnak	APN	19	9,013,698 (GRCm38)	missense	probably damaging	1.00
IGL01101:Ahnak	APN	19	9,012,887 (GRCm38)	intron	probably benign
IGL01118:Ahnak	APN	19	9,012,578 (GRCm38)	missense	probably damaging	1.00
IGL01288:Ahnak	APN	19	9,002,494 (GRCm38)	missense	possibly damaging	0.94
IGL01324:Ahnak	APN	19	9,003,032 (GRCm38)	missense	probably damaging	1.00
IGL01341:Ahnak	APN	19	9,011,703 (GRCm38)	missense	probably benign
IGL01541:Ahnak	APN	19	9,007,879 (GRCm38)	missense	possibly damaging	0.95
IGL01580:Ahnak	APN	19	9,002,839 (GRCm38)	missense	probably benign	0.02
IGL01595:Ahnak	APN	19	9,003,501 (GRCm38)	nonsense	probably null
IGL01746:Ahnak	APN	19	9,004,912 (GRCm38)	missense	possibly damaging	0.89
IGL01766:Ahnak	APN	19	9,000,118 (GRCm38)	missense	unknown
IGL01821:Ahnak	APN	19	9,012,118 (GRCm38)	missense	probably benign
IGL01913:Ahnak	APN	19	9,006,064 (GRCm38)	nonsense	probably null
IGL01934:Ahnak	APN	19	9,002,657 (GRCm38)	missense	probably damaging	1.00
IGL01940:Ahnak	APN	19	9,006,557 (GRCm38)	missense	probably benign	0.14
IGL01958:Ahnak	APN	19	9,014,909 (GRCm38)	missense	possibly damaging	0.59
IGL02145:Ahnak	APN	19	9,002,855 (GRCm38)	missense	probably benign	0.11
IGL02246:Ahnak	APN	19	9,008,268 (GRCm38)	missense	probably damaging	1.00
IGL02282:Ahnak	APN	19	9,005,987 (GRCm38)	missense	probably damaging	1.00
IGL02428:Ahnak	APN	19	9,014,833 (GRCm38)	missense	possibly damaging	0.83
IGL02442:Ahnak	APN	19	9,004,016 (GRCm38)	missense	probably damaging	1.00
IGL02474:Ahnak	APN	19	9,004,933 (GRCm38)	missense	probably benign	0.13
IGL02483:Ahnak	APN	19	9,003,308 (GRCm38)	missense	probably benign	0.01
IGL02616:Ahnak	APN	19	9,005,627 (GRCm38)	missense	probably benign	0.03
IGL02630:Ahnak	APN	19	9,012,077 (GRCm38)	missense	probably damaging	1.00
IGL02690:Ahnak	APN	19	9,012,584 (GRCm38)	nonsense	probably null
IGL02717:Ahnak	APN	19	9,002,387 (GRCm38)	missense	probably benign	0.00
IGL02721:Ahnak	APN	19	9,009,707 (GRCm38)	missense	probably benign	0.07
IGL02737:Ahnak	APN	19	9,004,593 (GRCm38)	missense	probably benign	0.17
IGL02850:Ahnak	APN	19	9,002,596 (GRCm38)	missense	probably benign	0.00
IGL03071:Ahnak	APN	19	9,011,918 (GRCm38)	missense	possibly damaging	0.63
IGL03072:Ahnak	APN	19	9,006,508 (GRCm38)	missense	probably benign	0.11
IGL03094:Ahnak	APN	19	9,003,547 (GRCm38)	missense	possibly damaging	0.64
IGL03140:Ahnak	APN	19	9,005,212 (GRCm38)	intron	probably benign
IGL03176:Ahnak	APN	19	9,002,449 (GRCm38)	missense	probably damaging	1.00
IGL03176:Ahnak	APN	19	9,008,166 (GRCm38)	missense	possibly damaging	0.56
IGL03189:Ahnak	APN	19	9,011,239 (GRCm38)	missense	possibly damaging	0.65
IGL03357:Ahnak	APN	19	9,009,325 (GRCm38)	intron	probably benign
IGL03371:Ahnak	APN	19	9,004,228 (GRCm38)	missense	possibly damaging	0.91
Eskimo	UTSW	19	9,009,574 (GRCm38)	missense	probably benign	0.31
Nanook	UTSW	19	9,003,231 (GRCm38)	missense	probably benign	0.42
Netsilik	UTSW	19	9,002,321 (GRCm38)	missense	probably benign	0.00
IGL03097:Ahnak	UTSW	19	9,002,387 (GRCm38)	missense	probably benign	0.00
PIT4403001:Ahnak	UTSW	19	9,006,176 (GRCm38)	missense	possibly damaging	0.87
R0054:Ahnak	UTSW	19	9,012,056 (GRCm38)	missense	probably damaging	1.00
R0094:Ahnak	UTSW	19	9,013,893 (GRCm38)	missense	probably benign	0.12
R0110:Ahnak	UTSW	19	9,018,232 (GRCm38)	nonsense	probably null
R0141:Ahnak	UTSW	19	9,006,680 (GRCm38)	missense	probably damaging	1.00
R0166:Ahnak	UTSW	19	9,005,725 (GRCm38)	missense	probably damaging	1.00
R0309:Ahnak	UTSW	19	9,002,495 (GRCm38)	missense	probably damaging	1.00
R0368:Ahnak	UTSW	19	9,008,350 (GRCm38)	nonsense	probably null
R0386:Ahnak	UTSW	19	9,011,144 (GRCm38)	missense	possibly damaging	0.94
R0401:Ahnak	UTSW	19	9,015,116 (GRCm38)	missense	probably benign	0.24
R0415:Ahnak	UTSW	19	9,012,871 (GRCm38)	intron	probably benign
R0463:Ahnak	UTSW	19	9,009,407 (GRCm38)	intron	probably benign
R0469:Ahnak	UTSW	19	9,018,232 (GRCm38)	nonsense	probably null
R0470:Ahnak	UTSW	19	9,008,967 (GRCm38)	missense	probably benign	0.29
R0487:Ahnak	UTSW	19	9,014,120 (GRCm38)	missense	probably damaging	0.99
R0487:Ahnak	UTSW	19	9,007,151 (GRCm38)	missense	probably benign	0.00
R0499:Ahnak	UTSW	19	9,000,264 (GRCm38)	splice site	probably benign
R0506:Ahnak	UTSW	19	9,009,128 (GRCm38)	missense	probably damaging	1.00
R0510:Ahnak	UTSW	19	9,018,232 (GRCm38)	nonsense	probably null
R0557:Ahnak	UTSW	19	9,001,944 (GRCm38)	missense	probably benign	0.10
R0570:Ahnak	UTSW	19	9,013,698 (GRCm38)	missense	probably damaging	1.00
R0610:Ahnak	UTSW	19	9,007,878 (GRCm38)	missense	probably benign	0.08
R0646:Ahnak	UTSW	19	9,013,402 (GRCm38)	nonsense	probably null
R0659:Ahnak	UTSW	19	9,015,002 (GRCm38)	missense	possibly damaging	0.60
R0791:Ahnak	UTSW	19	9,016,734 (GRCm38)	missense	probably benign	0.01
R0792:Ahnak	UTSW	19	9,016,734 (GRCm38)	missense	probably benign	0.01
R0840:Ahnak	UTSW	19	9,005,063 (GRCm38)	missense	probably damaging	1.00
R0847:Ahnak	UTSW	19	9,006,433 (GRCm38)	nonsense	probably null
R0941:Ahnak	UTSW	19	9,009,914 (GRCm38)	missense	probably damaging	1.00
R0962:Ahnak	UTSW	19	9,012,848 (GRCm38)	intron	probably benign
R1017:Ahnak	UTSW	19	9,010,543 (GRCm38)	missense	probably damaging	0.99
R1037:Ahnak	UTSW	19	9,007,618 (GRCm38)	missense	probably benign	0.27
R1085:Ahnak	UTSW	19	9,013,125 (GRCm38)	missense	possibly damaging	0.50
R1113:Ahnak	UTSW	19	9,005,620 (GRCm38)	missense	probably benign	0.29
R1140:Ahnak	UTSW	19	9,004,245 (GRCm38)	missense	probably damaging	1.00
R1158:Ahnak	UTSW	19	9,013,926 (GRCm38)	missense	probably benign	0.00
R1218:Ahnak	UTSW	19	9,015,619 (GRCm38)	missense	probably damaging	1.00
R1225:Ahnak	UTSW	19	9,002,883 (GRCm38)	missense	probably damaging	1.00
R1245:Ahnak	UTSW	19	9,004,169 (GRCm38)	missense	probably benign	0.44
R1421:Ahnak	UTSW	19	9,015,631 (GRCm38)	missense	possibly damaging	0.95
R1447:Ahnak	UTSW	19	9,007,082 (GRCm38)	missense	probably damaging	0.98
R1464:Ahnak	UTSW	19	9,004,896 (GRCm38)	missense	probably damaging	1.00
R1464:Ahnak	UTSW	19	9,004,896 (GRCm38)	missense	probably damaging	1.00
R1466:Ahnak	UTSW	19	9,015,875 (GRCm38)	missense	probably damaging	1.00
R1466:Ahnak	UTSW	19	9,015,875 (GRCm38)	missense	probably damaging	1.00
R1471:Ahnak	UTSW	19	9,012,932 (GRCm38)	intron	probably benign
R1507:Ahnak	UTSW	19	9,010,077 (GRCm38)	missense	probably damaging	1.00
R1521:Ahnak	UTSW	19	9,004,728 (GRCm38)	missense	probably benign	0.11
R1568:Ahnak	UTSW	19	9,002,375 (GRCm38)	missense	probably damaging	0.98
R1569:Ahnak	UTSW	19	9,004,094 (GRCm38)	missense	possibly damaging	0.78
R1616:Ahnak	UTSW	19	9,008,987 (GRCm38)	missense	possibly damaging	0.94
R1638:Ahnak	UTSW	19	9,009,449 (GRCm38)	missense	probably benign	0.01
R1680:Ahnak	UTSW	19	9,009,963 (GRCm38)	missense	probably benign	0.05
R1713:Ahnak	UTSW	19	9,011,809 (GRCm38)	missense	possibly damaging	0.95
R1722:Ahnak	UTSW	19	9,010,655 (GRCm38)	missense	probably damaging	0.99
R1771:Ahnak	UTSW	19	9,013,753 (GRCm38)	missense	probably benign	0.24
R1795:Ahnak	UTSW	19	9,002,438 (GRCm38)	missense	possibly damaging	0.79
R1823:Ahnak	UTSW	19	9,004,905 (GRCm38)	missense	probably damaging	0.99
R1842:Ahnak	UTSW	19	9,005,867 (GRCm38)	missense	probably damaging	0.99
R1854:Ahnak	UTSW	19	9,013,832 (GRCm38)	missense	possibly damaging	0.61
R1856:Ahnak	UTSW	19	9,002,048 (GRCm38)	missense	possibly damaging	0.86
R1886:Ahnak	UTSW	19	9,015,979 (GRCm38)	missense	probably damaging	0.98
R1888:Ahnak	UTSW	19	9,007,088 (GRCm38)	missense	probably damaging	1.00
R1888:Ahnak	UTSW	19	9,007,088 (GRCm38)	missense	probably damaging	1.00
R1912:Ahnak	UTSW	19	9,017,881 (GRCm38)	missense	probably damaging	1.00
R1913:Ahnak	UTSW	19	9,007,922 (GRCm38)	missense	probably damaging	0.99
R1942:Ahnak	UTSW	19	9,015,083 (GRCm38)	missense	probably damaging	0.98
R1987:Ahnak	UTSW	19	9,015,251 (GRCm38)	missense	probably damaging	1.00
R2006:Ahnak	UTSW	19	9,007,075 (GRCm38)	missense	probably damaging	1.00
R2013:Ahnak	UTSW	19	9,014,573 (GRCm38)	missense	probably damaging	0.98
R2014:Ahnak	UTSW	19	9,013,181 (GRCm38)	missense	probably damaging	0.99
R2047:Ahnak	UTSW	19	9,014,300 (GRCm38)	missense	possibly damaging	0.67
R2048:Ahnak	UTSW	19	9,007,056 (GRCm38)	missense	probably damaging	0.99
R2060:Ahnak	UTSW	19	9,008,041 (GRCm38)	missense	probably benign	0.08
R2083:Ahnak	UTSW	19	9,011,557 (GRCm38)	missense	probably damaging	1.00
R2157:Ahnak	UTSW	19	9,000,684 (GRCm38)	missense	possibly damaging	0.92
R2167:Ahnak	UTSW	19	9,011,494 (GRCm38)	nonsense	probably null
R2208:Ahnak	UTSW	19	9,017,732 (GRCm38)	missense	probably benign	0.00
R2224:Ahnak	UTSW	19	9,012,991 (GRCm38)	intron	probably benign
R2268:Ahnak	UTSW	19	9,010,574 (GRCm38)	missense	possibly damaging	0.66
R2420:Ahnak	UTSW	19	9,009,256 (GRCm38)	missense	possibly damaging	0.89
R2426:Ahnak	UTSW	19	9,002,851 (GRCm38)	missense	possibly damaging	0.81
R2910:Ahnak	UTSW	19	9,011,654 (GRCm38)	missense	probably damaging	0.99
R2911:Ahnak	UTSW	19	9,011,654 (GRCm38)	missense	probably damaging	0.99
R2981:Ahnak	UTSW	19	9,000,148 (GRCm38)	missense	probably damaging	0.97
R3151:Ahnak	UTSW	19	9,009,944 (GRCm38)	missense	probably benign	0.12
R3155:Ahnak	UTSW	19	9,010,177 (GRCm38)	missense	possibly damaging	0.49
R3422:Ahnak	UTSW	19	9,006,752 (GRCm38)	missense	probably benign	0.05
R3422:Ahnak	UTSW	19	9,005,708 (GRCm38)	missense	probably benign	0.39
R3430:Ahnak	UTSW	19	9,006,958 (GRCm38)	missense	probably benign	0.42
R3433:Ahnak	UTSW	19	9,009,994 (GRCm38)	missense	probably benign	0.01
R3711:Ahnak	UTSW	19	9,007,898 (GRCm38)	missense	probably benign
R3723:Ahnak	UTSW	19	9,016,853 (GRCm38)	missense	possibly damaging	0.79
R3775:Ahnak	UTSW	19	9,009,023 (GRCm38)	missense	possibly damaging	0.91
R3858:Ahnak	UTSW	19	9,010,859 (GRCm38)	missense	possibly damaging	0.82
R3859:Ahnak	UTSW	19	9,010,859 (GRCm38)	missense	possibly damaging	0.82
R3922:Ahnak	UTSW	19	9,006,328 (GRCm38)	missense	probably benign	0.20
R3924:Ahnak	UTSW	19	9,006,328 (GRCm38)	missense	probably benign	0.20
R3926:Ahnak	UTSW	19	9,006,328 (GRCm38)	missense	probably benign	0.20
R4026:Ahnak	UTSW	19	9,011,299 (GRCm38)	missense	probably damaging	0.97
R4051:Ahnak	UTSW	19	9,014,327 (GRCm38)	missense	probably damaging	1.00
R4209:Ahnak	UTSW	19	9,002,600 (GRCm38)	missense	probably damaging	1.00
R4234:Ahnak	UTSW	19	9,000,786 (GRCm38)	nonsense	probably null
R4237:Ahnak	UTSW	19	9,001,783 (GRCm38)	missense	probably benign	0.02
R4285:Ahnak	UTSW	19	9,016,839 (GRCm38)	nonsense	probably null
R4331:Ahnak	UTSW	19	9,015,820 (GRCm38)	missense	probably damaging	1.00
R4342:Ahnak	UTSW	19	9,012,083 (GRCm38)	missense	possibly damaging	0.79
R4430:Ahnak	UTSW	19	9,003,040 (GRCm38)	missense	probably benign	0.00
R4554:Ahnak	UTSW	19	9,014,930 (GRCm38)	missense	probably damaging	1.00
R4602:Ahnak	UTSW	19	9,010,825 (GRCm38)	missense	possibly damaging	0.66
R4612:Ahnak	UTSW	19	9,003,724 (GRCm38)	missense	probably benign	0.44
R4655:Ahnak	UTSW	19	9,008,701 (GRCm38)	missense	probably damaging	1.00
R4656:Ahnak	UTSW	19	9,004,855 (GRCm38)	missense	possibly damaging	0.80
R4700:Ahnak	UTSW	19	9,004,681 (GRCm38)	missense	probably benign	0.02
R4704:Ahnak	UTSW	19	9,012,258 (GRCm38)	intron	probably benign
R4704:Ahnak	UTSW	19	9,013,181 (GRCm38)	missense	probably damaging	0.99
R4705:Ahnak	UTSW	19	9,016,906 (GRCm38)	missense	probably benign	0.07
R4707:Ahnak	UTSW	19	9,016,735 (GRCm38)	missense	probably benign	0.03
R4733:Ahnak	UTSW	19	9,007,301 (GRCm38)	missense	probably damaging	1.00
R4778:Ahnak	UTSW	19	9,011,975 (GRCm38)	missense	possibly damaging	0.79
R4782:Ahnak	UTSW	19	9,012,499 (GRCm38)	intron	probably benign
R4832:Ahnak	UTSW	19	9,012,460 (GRCm38)	intron	probably benign
R4882:Ahnak	UTSW	19	9,005,897 (GRCm38)	missense	probably damaging	0.98
R4884:Ahnak	UTSW	19	9,012,754 (GRCm38)	intron	probably benign
R4895:Ahnak	UTSW	19	9,017,441 (GRCm38)	missense	probably benign	0.43
R4930:Ahnak	UTSW	19	9,010,967 (GRCm38)	missense	possibly damaging	0.79
R4951:Ahnak	UTSW	19	9,017,835 (GRCm38)	missense	probably damaging	1.00
R4968:Ahnak	UTSW	19	9,015,100 (GRCm38)	missense	probably damaging	1.00
R5026:Ahnak	UTSW	19	9,010,631 (GRCm38)	missense	possibly damaging	0.46
R5050:Ahnak	UTSW	19	9,012,458 (GRCm38)	intron	probably benign
R5073:Ahnak	UTSW	19	9,003,231 (GRCm38)	missense	probably benign	0.42
R5110:Ahnak	UTSW	19	9,014,759 (GRCm38)	missense	probably damaging	1.00
R5119:Ahnak	UTSW	19	9,013,644 (GRCm38)	missense	probably benign	0.00
R5128:Ahnak	UTSW	19	9,017,087 (GRCm38)	missense	probably damaging	1.00
R5139:Ahnak	UTSW	19	9,004,655 (GRCm38)	missense	probably damaging	1.00
R5150:Ahnak	UTSW	19	9,010,904 (GRCm38)	missense	possibly damaging	0.46
R5151:Ahnak	UTSW	19	9,017,569 (GRCm38)	missense	probably benign	0.03
R5165:Ahnak	UTSW	19	9,015,665 (GRCm38)	missense	possibly damaging	0.95
R5236:Ahnak	UTSW	19	9,000,684 (GRCm38)	missense	possibly damaging	0.92
R5361:Ahnak	UTSW	19	9,015,341 (GRCm38)	missense	possibly damaging	0.92
R5366:Ahnak	UTSW	19	9,016,735 (GRCm38)	missense	possibly damaging	0.65
R5387:Ahnak	UTSW	19	9,003,691 (GRCm38)	missense	probably damaging	1.00
R5396:Ahnak	UTSW	19	9,007,175 (GRCm38)	missense	probably damaging	0.99
R5583:Ahnak	UTSW	19	9,006,917 (GRCm38)	missense	probably damaging	0.99
R5587:Ahnak	UTSW	19	9,009,476 (GRCm38)	missense	possibly damaging	0.88
R5620:Ahnak	UTSW	19	9,013,094 (GRCm38)	nonsense	probably null
R5643:Ahnak	UTSW	19	9,010,657 (GRCm38)	missense	possibly damaging	0.66
R5644:Ahnak	UTSW	19	9,010,657 (GRCm38)	missense	possibly damaging	0.66
R5657:Ahnak	UTSW	19	9,014,615 (GRCm38)	missense	probably damaging	0.99
R5688:Ahnak	UTSW	19	9,002,519 (GRCm38)	missense	probably benign	0.01
R5702:Ahnak	UTSW	19	9,001,840 (GRCm38)	missense	probably damaging	1.00
R5727:Ahnak	UTSW	19	9,016,747 (GRCm38)	missense	probably damaging	0.99
R5730:Ahnak	UTSW	19	9,010,253 (GRCm38)	missense	possibly damaging	0.81
R5755:Ahnak	UTSW	19	9,001,732 (GRCm38)	missense	probably benign	0.06
R5760:Ahnak	UTSW	19	9,013,562 (GRCm38)	missense	probably damaging	1.00
R5789:Ahnak	UTSW	19	9,002,321 (GRCm38)	missense	probably benign	0.00
R5790:Ahnak	UTSW	19	9,015,248 (GRCm38)	missense	probably damaging	0.99
R5795:Ahnak	UTSW	19	9,012,382 (GRCm38)	nonsense	probably null
R5808:Ahnak	UTSW	19	9,010,235 (GRCm38)	missense	possibly damaging	0.91
R5867:Ahnak	UTSW	19	9,010,052 (GRCm38)	missense	probably damaging	0.99
R5878:Ahnak	UTSW	19	9,008,342 (GRCm38)	missense	probably damaging	1.00
R5898:Ahnak	UTSW	19	9,018,211 (GRCm38)	missense	probably damaging	1.00
R5898:Ahnak	UTSW	19	9,013,767 (GRCm38)	missense	possibly damaging	0.63
R5912:Ahnak	UTSW	19	9,011,903 (GRCm38)	missense	probably damaging	0.99
R5935:Ahnak	UTSW	19	9,015,182 (GRCm38)	missense	possibly damaging	0.91
R5969:Ahnak	UTSW	19	9,016,585 (GRCm38)	missense	probably damaging	1.00
R5988:Ahnak	UTSW	19	9,009,347 (GRCm38)	intron	probably benign
R6000:Ahnak	UTSW	19	9,013,111 (GRCm38)	nonsense	probably null
R6005:Ahnak	UTSW	19	9,015,161 (GRCm38)	missense	possibly damaging	0.61
R6101:Ahnak	UTSW	19	9,004,099 (GRCm38)	missense	probably benign	0.20
R6105:Ahnak	UTSW	19	9,004,099 (GRCm38)	missense	probably benign	0.20
R6116:Ahnak	UTSW	19	9,012,963 (GRCm38)	intron	probably benign
R6209:Ahnak	UTSW	19	9,012,566 (GRCm38)	missense	probably damaging	1.00
R6240:Ahnak	UTSW	19	9,013,583 (GRCm38)	missense	probably damaging	1.00
R6255:Ahnak	UTSW	19	9,008,025 (GRCm38)	missense	possibly damaging	0.95
R6263:Ahnak	UTSW	19	9,018,277 (GRCm38)	missense	probably benign	0.03
R6287:Ahnak	UTSW	19	9,015,003 (GRCm38)	missense	probably benign	0.02
R6296:Ahnak	UTSW	19	9,003,305 (GRCm38)	missense	probably damaging	0.99
R6315:Ahnak	UTSW	19	9,006,626 (GRCm38)	missense	probably damaging	0.99
R6328:Ahnak	UTSW	19	9,007,148 (GRCm38)	missense	probably benign	0.11
R6331:Ahnak	UTSW	19	9,006,625 (GRCm38)	missense	probably benign	0.18
R6355:Ahnak	UTSW	19	9,008,762 (GRCm38)	missense	probably benign	0.02
R6409:Ahnak	UTSW	19	9,009,574 (GRCm38)	missense	probably benign	0.31
R6567:Ahnak	UTSW	19	9,008,806 (GRCm38)	missense	probably benign	0.27
R6572:Ahnak	UTSW	19	9,007,976 (GRCm38)	missense	probably damaging	0.99
R6574:Ahnak	UTSW	19	9,017,047 (GRCm38)	missense	probably benign	0.04
R6590:Ahnak	UTSW	19	9,009,581 (GRCm38)	missense	probably benign	0.29
R6620:Ahnak	UTSW	19	9,015,310 (GRCm38)	missense	possibly damaging	0.95
R6690:Ahnak	UTSW	19	9,009,581 (GRCm38)	missense	probably benign	0.29
R6731:Ahnak	UTSW	19	9,011,562 (GRCm38)	missense	possibly damaging	0.85
R6756:Ahnak	UTSW	19	9,007,561 (GRCm38)	missense	possibly damaging	0.59
R6846:Ahnak	UTSW	19	9,011,857 (GRCm38)	missense	possibly damaging	0.66
R6854:Ahnak	UTSW	19	9,015,235 (GRCm38)	missense	probably damaging	1.00
R6857:Ahnak	UTSW	19	9,037,168 (GRCm38)	nonsense	probably null
R6863:Ahnak	UTSW	19	9,012,365 (GRCm38)	intron	probably benign
R6876:Ahnak	UTSW	19	9,014,120 (GRCm38)	missense	probably damaging	0.99
R6958:Ahnak	UTSW	19	9,015,215 (GRCm38)	missense	possibly damaging	0.88
R7126:Ahnak	UTSW	19	9,002,359 (GRCm38)	missense	possibly damaging	0.61
R7181:Ahnak	UTSW	19	9,013,488 (GRCm38)	missense	probably damaging	1.00
R7183:Ahnak	UTSW	19	9,017,668 (GRCm38)	missense	probably damaging	1.00
R7202:Ahnak	UTSW	19	9,017,799 (GRCm38)	missense	probably damaging	1.00
R7235:Ahnak	UTSW	19	9,012,488 (GRCm38)	missense	unknown
R7241:Ahnak	UTSW	19	9,009,031 (GRCm38)	missense	possibly damaging	0.65
R7269:Ahnak	UTSW	19	9,006,617 (GRCm38)	missense	probably damaging	1.00
R7311:Ahnak	UTSW	19	9,002,143 (GRCm38)	missense	probably benign	0.04
R7311:Ahnak	UTSW	19	9,009,827 (GRCm38)	missense	possibly damaging	0.56
R7329:Ahnak	UTSW	19	9,001,792 (GRCm38)	missense	probably damaging	0.99
R7339:Ahnak	UTSW	19	9,008,165 (GRCm38)	missense	possibly damaging	0.75
R7390:Ahnak	UTSW	19	9,003,205 (GRCm38)	missense	probably benign	0.02
R7400:Ahnak	UTSW	19	9,014,613 (GRCm38)	missense	probably damaging	0.99
R7444:Ahnak	UTSW	19	9,007,423 (GRCm38)	missense	probably benign	0.08
R7483:Ahnak	UTSW	19	9,004,822 (GRCm38)	missense	probably damaging	1.00
R7498:Ahnak	UTSW	19	9,012,019 (GRCm38)	missense	probably benign	0.14
R7521:Ahnak	UTSW	19	9,002,351 (GRCm38)	missense	possibly damaging	0.89
R7522:Ahnak	UTSW	19	9,002,322 (GRCm38)	missense	probably benign	0.01
R7552:Ahnak	UTSW	19	9,006,824 (GRCm38)	missense	probably benign	0.18
R7563:Ahnak	UTSW	19	9,011,165 (GRCm38)	missense	probably damaging	0.99
R7565:Ahnak	UTSW	19	9,016,156 (GRCm38)	missense	probably benign	0.05
R7571:Ahnak	UTSW	19	9,000,786 (GRCm38)	nonsense	probably null
R7583:Ahnak	UTSW	19	9,006,093 (GRCm38)	missense	possibly damaging	0.90
R7600:Ahnak	UTSW	19	9,004,574 (GRCm38)	missense	possibly damaging	0.89
R7771:Ahnak	UTSW	19	9,015,047 (GRCm38)	missense	probably damaging	0.99
R7787:Ahnak	UTSW	19	9,009,315 (GRCm38)	missense	unknown
R7827:Ahnak	UTSW	19	9,005,344 (GRCm38)	nonsense	probably null
R7857:Ahnak	UTSW	19	9,007,468 (GRCm38)	missense	probably damaging	0.97
R7916:Ahnak	UTSW	19	9,005,832 (GRCm38)	missense	possibly damaging	0.66
R7939:Ahnak	UTSW	19	9,014,084 (GRCm38)	nonsense	probably null
R7959:Ahnak	UTSW	19	9,010,649 (GRCm38)	missense	possibly damaging	0.46
R7962:Ahnak	UTSW	19	9,012,800 (GRCm38)	missense	unknown
R7979:Ahnak	UTSW	19	9,011,432 (GRCm38)	missense	probably damaging	1.00
R8006:Ahnak	UTSW	19	9,012,083 (GRCm38)	missense	possibly damaging	0.79
R8013:Ahnak	UTSW	19	9,009,335 (GRCm38)	missense	unknown
R8033:Ahnak	UTSW	19	9,003,710 (GRCm38)	missense	probably benign	0.10
R8124:Ahnak	UTSW	19	9,007,123 (GRCm38)	missense	probably damaging	0.99
R8125:Ahnak	UTSW	19	9,011,876 (GRCm38)	missense	possibly damaging	0.95
R8129:Ahnak	UTSW	19	9,000,100 (GRCm38)	start codon destroyed	not run
R8151:Ahnak	UTSW	19	9,004,679 (GRCm38)	missense	possibly damaging	0.59
R8190:Ahnak	UTSW	19	9,002,255 (GRCm38)	missense	probably benign	0.01
R8221:Ahnak	UTSW	19	9,010,436 (GRCm38)	nonsense	probably null
R8241:Ahnak	UTSW	19	9,007,295 (GRCm38)	missense	probably benign	0.15
R8244:Ahnak	UTSW	19	9,015,673 (GRCm38)	missense	probably benign	0.44
R8248:Ahnak	UTSW	19	9,001,946 (GRCm38)	missense	probably damaging	1.00
R8261:Ahnak	UTSW	19	9,005,453 (GRCm38)	missense	probably damaging	1.00
R8330:Ahnak	UTSW	19	9,009,662 (GRCm38)	missense	possibly damaging	0.86
R8380:Ahnak	UTSW	19	9,017,855 (GRCm38)	missense	probably benign	0.05
R8407:Ahnak	UTSW	19	9,015,673 (GRCm38)	missense	probably benign	0.44
R8409:Ahnak	UTSW	19	9,015,673 (GRCm38)	missense	probably benign	0.44
R8463:Ahnak	UTSW	19	9,008,749 (GRCm38)	missense	probably benign	0.07
R8511:Ahnak	UTSW	19	9,012,355 (GRCm38)	missense	unknown
R8528:Ahnak	UTSW	19	9,007,728 (GRCm38)	missense	probably damaging	1.00
R8549:Ahnak	UTSW	19	9,011,483 (GRCm38)	missense	probably damaging	1.00
R8674:Ahnak	UTSW	19	9,005,996 (GRCm38)	missense	probably damaging	0.98
R8716:Ahnak	UTSW	19	9,009,074 (GRCm38)	missense	probably damaging	1.00
R8722:Ahnak	UTSW	19	9,013,346 (GRCm38)	nonsense	probably null
R8751:Ahnak	UTSW	19	9,010,145 (GRCm38)	missense	probably damaging	1.00
R8752:Ahnak	UTSW	19	9,015,537 (GRCm38)	missense	probably damaging	1.00
R8783:Ahnak	UTSW	19	9,011,473 (GRCm38)	missense	probably damaging	1.00
R8844:Ahnak	UTSW	19	9,006,890 (GRCm38)	missense	probably damaging	1.00
R8859:Ahnak	UTSW	19	9,007,203 (GRCm38)	missense	probably damaging	1.00
R8882:Ahnak	UTSW	19	9,000,742 (GRCm38)	missense	probably damaging	1.00
R8907:Ahnak	UTSW	19	9,009,088 (GRCm38)	missense	probably benign	0.24
R8938:Ahnak	UTSW	19	9,011,735 (GRCm38)	missense	probably benign	0.00
R8975:Ahnak	UTSW	19	9,012,737 (GRCm38)	missense	probably damaging	1.00
R8983:Ahnak	UTSW	19	9,004,113 (GRCm38)	missense	possibly damaging	0.75
R9017:Ahnak	UTSW	19	9,010,123 (GRCm38)	missense	probably damaging	1.00
R9027:Ahnak	UTSW	19	9,007,253 (GRCm38)	missense	possibly damaging	0.94
R9081:Ahnak	UTSW	19	9,008,526 (GRCm38)	missense	possibly damaging	0.81
R9104:Ahnak	UTSW	19	9,010,347 (GRCm38)	missense	probably benign	0.01
R9112:Ahnak	UTSW	19	9,009,785 (GRCm38)	missense	probably damaging	0.98
R9145:Ahnak	UTSW	19	9,014,923 (GRCm38)	missense	probably benign	0.38
R9189:Ahnak	UTSW	19	9,010,883 (GRCm38)	missense	possibly damaging	0.92
R9221:Ahnak	UTSW	19	9,012,579 (GRCm38)	missense	probably damaging	1.00
R9261:Ahnak	UTSW	19	9,016,139 (GRCm38)	missense	possibly damaging	0.63
R9299:Ahnak	UTSW	19	9,012,460 (GRCm38)	intron	probably benign
R9325:Ahnak	UTSW	19	9,013,893 (GRCm38)	missense	probably benign	0.12
R9337:Ahnak	UTSW	19	9,012,460 (GRCm38)	intron	probably benign
R9340:Ahnak	UTSW	19	9,017,047 (GRCm38)	missense	probably benign	0.04
R9351:Ahnak	UTSW	19	9,007,868 (GRCm38)	missense	probably damaging	1.00
R9416:Ahnak	UTSW	19	9,012,902 (GRCm38)	missense	unknown
R9462:Ahnak	UTSW	19	9,003,935 (GRCm38)	missense	probably damaging	0.96
R9469:Ahnak	UTSW	19	9,010,861 (GRCm38)	missense	probably damaging	1.00
R9485:Ahnak	UTSW	19	9,002,074 (GRCm38)	missense	probably benign	0.16
R9503:Ahnak	UTSW	19	9,010,094 (GRCm38)	missense	probably damaging	1.00
R9524:Ahnak	UTSW	19	9,037,253 (GRCm38)	missense
R9534:Ahnak	UTSW	19	9,003,612 (GRCm38)	missense	probably benign	0.20
R9598:Ahnak	UTSW	19	9,003,785 (GRCm38)	missense	probably benign	0.42
R9611:Ahnak	UTSW	19	9,011,798 (GRCm38)	missense	probably damaging	0.99
R9624:Ahnak	UTSW	19	9,012,482 (GRCm38)	missense	unknown
R9649:Ahnak	UTSW	19	9,008,422 (GRCm38)	nonsense	probably null
R9683:Ahnak	UTSW	19	9,007,355 (GRCm38)	missense	possibly damaging	0.94
R9691:Ahnak	UTSW	19	9,011,726 (GRCm38)	missense	possibly damaging	0.49
R9712:Ahnak	UTSW	19	9,007,029 (GRCm38)	small deletion	probably benign
R9712:Ahnak	UTSW	19	9,007,028 (GRCm38)	small deletion	probably benign
R9713:Ahnak	UTSW	19	9,007,029 (GRCm38)	small deletion	probably benign
R9715:Ahnak	UTSW	19	9,007,029 (GRCm38)	small deletion	probably benign
R9725:Ahnak	UTSW	19	9,014,243 (GRCm38)	missense	probably damaging	1.00
R9725:Ahnak	UTSW	19	9,004,169 (GRCm38)	missense	probably benign	0.44
R9747:Ahnak	UTSW	19	9,010,177 (GRCm38)	missense	possibly damaging	0.49
R9798:Ahnak	UTSW	19	9,013,619 (GRCm38)	missense	probably damaging	0.99
RF007:Ahnak	UTSW	19	9,013,601 (GRCm38)	missense	possibly damaging	0.45
X0021:Ahnak	UTSW	19	9,013,619 (GRCm38)	missense	probably damaging	0.99
X0027:Ahnak	UTSW	19	9,012,037 (GRCm38)	missense	probably damaging	1.00
Z1088:Ahnak	UTSW	19	9,016,082 (GRCm38)	missense	probably damaging	0.99
Z1176:Ahnak	UTSW	19	9,008,856 (GRCm38)	missense	probably damaging	0.97
Z1177:Ahnak	UTSW	19	9,017,468 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GAGATAGATGCTTCTGTGCCAG -3'
(R):5'- GATGCAAGTCCACATCAGGC -3'

Sequencing Primer
(F):5'- TGATCTCAGAGGCCCTCAAGTTG -3'
(R):5'- TCCACATCAGGCATGGAGATCTTAG -3'

Posted On

2015-11-11