Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02104:Trank1'

279900

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Trank1

Ensembl Gene

ENSMUSG00000062296

Gene Name

tetratricopeptide repeat and ankyrin repeat containing 1

Synonyms

LOC235639, C030048J01Rik, A230061D21Rik, Lba1

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02104

Quality Score

Status

Chromosome

Chromosomal Location

111140807-111224843 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 111219780 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 2172 (D2172E)

Ref Sequence

ENSEMBL: ENSMUSP00000077697 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078626]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000078626
AA Change: D2172E

PolyPhen 2 Score 0.851 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000077697
Gene: ENSMUSG00000062296
AA Change: D2172E

Domain	Start	End	E-Value	Type
low complexity region	4	30	N/A	INTRINSIC
low complexity region	34	52	N/A	INTRINSIC
low complexity region	113	129	N/A	INTRINSIC
Blast:TPR	144	177	1e-15	BLAST
Blast:TPR	178	209	8e-13	BLAST
Blast:ANK	332	361	1e-6	BLAST
ANK	369	405	5.29e0	SMART
ANK	538	567	2.11e2	SMART
ANK	572	609	7.29e2	SMART
ANK	621	652	1.21e2	SMART
low complexity region	887	895	N/A	INTRINSIC
low complexity region	1152	1172	N/A	INTRINSIC
Blast:AAA	1351	1569	1e-6	BLAST
low complexity region	2166	2177	N/A	INTRINSIC
low complexity region	2395	2411	N/A	INTRINSIC
low complexity region	2636	2649	N/A	INTRINSIC
low complexity region	2966	2983	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196945

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197650

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198890

Coding Region Coverage

Validation Efficiency

Allele List at MGI

All alleles(2) : Targeted, other(2)

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933440M02Rik	T	C	7: 124,930,714 (GRCm39)		noncoding transcript	Het
Abcb5	T	A	12: 118,904,415 (GRCm39)	Q125L	probably damaging	Het
Acap3	G	A	4: 155,989,542 (GRCm39)	R662H	probably damaging	Het
Aox4	T	A	1: 58,275,816 (GRCm39)		probably benign	Het
Aqp6	T	C	15: 99,502,159 (GRCm39)	S285P	probably benign	Het
Arhgef5	A	T	6: 43,249,345 (GRCm39)	Q32L	probably damaging	Het
B3gnt6	G	T	7: 97,843,308 (GRCm39)	D217E	probably damaging	Het
Cfap251	T	A	5: 123,440,761 (GRCm39)	L1106*	probably null	Het
Chd6	T	C	2: 160,819,432 (GRCm39)	I1338V	probably benign	Het
Clic6	A	G	16: 92,295,367 (GRCm39)	E9G	possibly damaging	Het
Col11a1	T	A	3: 113,975,046 (GRCm39)		probably null	Het
Dcdc2b	T	A	4: 129,504,867 (GRCm39)	D88V	probably benign	Het
Dis3l	T	A	9: 64,217,611 (GRCm39)	K791N	possibly damaging	Het
Dmxl2	A	T	9: 54,311,299 (GRCm39)	Y1008*	probably null	Het
Dnah11	A	G	12: 118,156,125 (GRCm39)	V175A	probably benign	Het
Efl1	A	G	7: 82,307,263 (GRCm39)		probably null	Het
Fam117b	C	T	1: 59,988,278 (GRCm39)	T219I	probably benign	Het
Fgf21	T	A	7: 45,264,648 (GRCm39)	Q28L	probably benign	Het
Folh1	T	C	7: 86,393,638 (GRCm39)	Q391R	possibly damaging	Het
Gars1	A	G	6: 55,054,682 (GRCm39)	D663G	probably damaging	Het
Lats2	A	G	14: 57,971,469 (GRCm39)	F69L	probably damaging	Het
Lrp2	C	T	2: 69,340,762 (GRCm39)	V1038M	probably damaging	Het
Map3k1	A	T	13: 111,892,777 (GRCm39)	V826E	probably damaging	Het
Mapkap1	T	A	2: 34,513,482 (GRCm39)	Y497*	probably null	Het
Mast3	T	C	8: 71,240,550 (GRCm39)	I296V	possibly damaging	Het
Mon1a	T	G	9: 107,778,814 (GRCm39)	L346R	probably damaging	Het
Mphosph8	T	C	14: 56,912,036 (GRCm39)	L353S	probably benign	Het
Muc5ac	T	C	7: 141,364,815 (GRCm39)	Y2634H	probably damaging	Het
Mylk	A	G	16: 34,635,805 (GRCm39)	T9A	probably benign	Het
Or10j2	T	C	1: 173,098,603 (GRCm39)	V287A	probably damaging	Het
Or14j8	A	C	17: 38,263,182 (GRCm39)	H244Q	probably damaging	Het
Or55b3	C	A	7: 102,126,544 (GRCm39)	V178F	probably damaging	Het
Or5an6	T	A	19: 12,372,263 (GRCm39)	V212D	probably damaging	Het
Or5b122	T	A	19: 13,562,968 (GRCm39)	M57K	probably damaging	Het
Or5m8	G	T	2: 85,822,730 (GRCm39)	D190Y	probably damaging	Het
Or7g25	A	T	9: 19,160,166 (GRCm39)	H176Q	probably benign	Het
Pabpc2	A	C	18: 39,907,936 (GRCm39)	Q400H	possibly damaging	Het
Pigg	A	G	5: 108,489,963 (GRCm39)	Y856C	probably damaging	Het
Plekhn1	A	T	4: 156,306,865 (GRCm39)	V508E	probably benign	Het
Pom121l2	C	A	13: 22,166,445 (GRCm39)	H239N	possibly damaging	Het
Prdm2	A	G	4: 142,859,997 (GRCm39)	S1098P	probably benign	Het
Rnf212	A	G	5: 108,895,306 (GRCm39)	I41T	possibly damaging	Het
Rngtt	A	G	4: 33,320,517 (GRCm39)		probably null	Het
Rpn2	C	T	2: 157,163,747 (GRCm39)	T613M	probably damaging	Het
Scd4	G	T	19: 44,333,186 (GRCm39)	V304F	possibly damaging	Het
Sez6l	A	G	5: 112,574,630 (GRCm39)		probably benign	Het
Shroom3	A	G	5: 93,088,248 (GRCm39)	R158G	probably benign	Het
Stil	T	C	4: 114,898,679 (GRCm39)	L1103P	probably damaging	Het
Tanc2	T	C	11: 105,670,959 (GRCm39)		probably benign	Het
Tmc1	C	T	19: 20,809,818 (GRCm39)	D255N	probably benign	Het
Tyro3	G	A	2: 119,643,681 (GRCm39)	R718H	probably damaging	Het
Vamp2	C	A	11: 68,981,483 (GRCm39)	F114L	probably benign	Het

Other mutations in Trank1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00234:Trank1	APN	9	111,221,677 (GRCm39)	missense	probably damaging	1.00
IGL00467:Trank1	APN	9	111,193,734 (GRCm39)	splice site	probably benign
IGL00569:Trank1	APN	9	111,174,579 (GRCm39)	missense	possibly damaging	0.69
IGL00585:Trank1	APN	9	111,178,358 (GRCm39)	missense	possibly damaging	0.82
IGL01070:Trank1	APN	9	111,195,861 (GRCm39)	missense	probably damaging	1.00
IGL01134:Trank1	APN	9	111,220,849 (GRCm39)	missense	probably benign
IGL01154:Trank1	APN	9	111,215,468 (GRCm39)	missense	probably benign	0.00
IGL01355:Trank1	APN	9	111,194,588 (GRCm39)	missense	possibly damaging	0.94
IGL01407:Trank1	APN	9	111,193,790 (GRCm39)	missense	probably damaging	0.99
IGL01410:Trank1	APN	9	111,194,117 (GRCm39)	missense	probably benign	0.00
IGL01410:Trank1	APN	9	111,194,327 (GRCm39)	missense	probably benign	0.00
IGL01504:Trank1	APN	9	111,202,612 (GRCm39)	missense	probably damaging	1.00
IGL01744:Trank1	APN	9	111,178,431 (GRCm39)	missense	probably damaging	1.00
IGL02043:Trank1	APN	9	111,193,028 (GRCm39)	missense	probably damaging	0.98
IGL02193:Trank1	APN	9	111,196,344 (GRCm39)	missense	probably benign	0.43
IGL02581:Trank1	APN	9	111,212,193 (GRCm39)	missense	probably benign	0.00
IGL02630:Trank1	APN	9	111,202,143 (GRCm39)	missense	possibly damaging	0.70
IGL02839:Trank1	APN	9	111,193,824 (GRCm39)	missense	probably damaging	1.00
IGL02897:Trank1	APN	9	111,196,585 (GRCm39)	missense	probably damaging	0.99
IGL03065:Trank1	APN	9	111,219,361 (GRCm39)	missense	possibly damaging	0.64
IGL03123:Trank1	APN	9	111,196,475 (GRCm39)	missense	probably damaging	1.00
IGL03143:Trank1	APN	9	111,195,155 (GRCm39)	missense	probably damaging	1.00
IGL03323:Trank1	APN	9	111,181,184 (GRCm39)	missense	probably damaging	1.00
1mM(1):Trank1	UTSW	9	111,222,049 (GRCm39)	missense	probably damaging	1.00
PIT4486001:Trank1	UTSW	9	111,219,175 (GRCm39)	missense	probably damaging	1.00
PIT4812001:Trank1	UTSW	9	111,176,980 (GRCm39)	missense	probably damaging	1.00
R0035:Trank1	UTSW	9	111,195,844 (GRCm39)	missense	probably benign	0.00
R0064:Trank1	UTSW	9	111,172,263 (GRCm39)	missense	probably damaging	1.00
R0064:Trank1	UTSW	9	111,172,263 (GRCm39)	missense	probably damaging	1.00
R0089:Trank1	UTSW	9	111,221,978 (GRCm39)	missense	probably benign	0.00
R0207:Trank1	UTSW	9	111,195,321 (GRCm39)	missense	probably damaging	1.00
R0255:Trank1	UTSW	9	111,195,092 (GRCm39)	missense	possibly damaging	0.92
R0334:Trank1	UTSW	9	111,222,008 (GRCm39)	missense	probably damaging	1.00
R0334:Trank1	UTSW	9	111,194,421 (GRCm39)	missense	probably benign	0.00
R0383:Trank1	UTSW	9	111,220,545 (GRCm39)	missense	probably benign	0.08
R0421:Trank1	UTSW	9	111,220,907 (GRCm39)	missense	probably damaging	1.00
R0494:Trank1	UTSW	9	111,220,361 (GRCm39)	missense	probably benign	0.19
R0518:Trank1	UTSW	9	111,162,876 (GRCm39)	missense	probably damaging	1.00
R0560:Trank1	UTSW	9	111,220,154 (GRCm39)	missense	possibly damaging	0.88
R0637:Trank1	UTSW	9	111,219,509 (GRCm39)	missense	probably damaging	1.00
R0731:Trank1	UTSW	9	111,194,556 (GRCm39)	missense	probably damaging	1.00
R0761:Trank1	UTSW	9	111,195,681 (GRCm39)	missense	probably damaging	1.00
R0766:Trank1	UTSW	9	111,176,537 (GRCm39)	missense	probably benign	0.45
R0827:Trank1	UTSW	9	111,178,485 (GRCm39)	unclassified	probably benign
R1005:Trank1	UTSW	9	111,162,789 (GRCm39)	missense	probably benign	0.13
R1108:Trank1	UTSW	9	111,194,375 (GRCm39)	missense	probably benign	0.00
R1155:Trank1	UTSW	9	111,196,038 (GRCm39)	missense	possibly damaging	0.95
R1470:Trank1	UTSW	9	111,172,300 (GRCm39)	missense	possibly damaging	0.91
R1470:Trank1	UTSW	9	111,172,300 (GRCm39)	missense	possibly damaging	0.91
R1596:Trank1	UTSW	9	111,195,358 (GRCm39)	missense	possibly damaging	0.93
R1601:Trank1	UTSW	9	111,202,545 (GRCm39)	missense	probably damaging	1.00
R1751:Trank1	UTSW	9	111,220,547 (GRCm39)	missense	probably benign
R1754:Trank1	UTSW	9	111,221,939 (GRCm39)	missense	probably benign	0.00
R1767:Trank1	UTSW	9	111,220,547 (GRCm39)	missense	probably benign
R1768:Trank1	UTSW	9	111,221,995 (GRCm39)	missense	probably damaging	0.96
R1809:Trank1	UTSW	9	111,221,893 (GRCm39)	missense	probably benign	0.34
R1912:Trank1	UTSW	9	111,219,777 (GRCm39)	missense	probably benign	0.00
R1920:Trank1	UTSW	9	111,176,996 (GRCm39)	critical splice donor site	probably null
R1960:Trank1	UTSW	9	111,220,696 (GRCm39)	missense	probably damaging	1.00
R1993:Trank1	UTSW	9	111,207,900 (GRCm39)	missense	probably benign	0.20
R2012:Trank1	UTSW	9	111,194,096 (GRCm39)	missense	probably benign
R2025:Trank1	UTSW	9	111,221,107 (GRCm39)	missense	probably benign	0.01
R2050:Trank1	UTSW	9	111,193,856 (GRCm39)	missense	probably damaging	1.00
R2857:Trank1	UTSW	9	111,196,001 (GRCm39)	missense	probably benign	0.00
R2912:Trank1	UTSW	9	111,221,551 (GRCm39)	missense	probably damaging	0.98
R2962:Trank1	UTSW	9	111,181,148 (GRCm39)	missense	probably damaging	1.00
R3030:Trank1	UTSW	9	111,220,598 (GRCm39)	missense	possibly damaging	0.63
R3821:Trank1	UTSW	9	111,207,887 (GRCm39)	missense	probably damaging	1.00
R3822:Trank1	UTSW	9	111,207,887 (GRCm39)	missense	probably damaging	1.00
R3892:Trank1	UTSW	9	111,193,827 (GRCm39)	missense	probably benign	0.03
R4105:Trank1	UTSW	9	111,181,265 (GRCm39)	missense	probably damaging	1.00
R4166:Trank1	UTSW	9	111,202,592 (GRCm39)	nonsense	probably null
R4237:Trank1	UTSW	9	111,196,103 (GRCm39)	missense	probably benign	0.04
R4239:Trank1	UTSW	9	111,196,103 (GRCm39)	missense	probably benign	0.04
R4394:Trank1	UTSW	9	111,194,265 (GRCm39)	missense	possibly damaging	0.86
R4417:Trank1	UTSW	9	111,195,036 (GRCm39)	missense	probably benign	0.17
R4611:Trank1	UTSW	9	111,191,329 (GRCm39)	missense	probably damaging	1.00
R4694:Trank1	UTSW	9	111,221,129 (GRCm39)	missense	probably benign	0.40
R4731:Trank1	UTSW	9	111,219,478 (GRCm39)	missense	probably damaging	1.00
R4843:Trank1	UTSW	9	111,195,146 (GRCm39)	missense	probably benign	0.00
R4852:Trank1	UTSW	9	111,220,963 (GRCm39)	missense	possibly damaging	0.68
R4859:Trank1	UTSW	9	111,194,078 (GRCm39)	missense	probably benign	0.17
R4868:Trank1	UTSW	9	111,194,709 (GRCm39)	missense	probably damaging	1.00
R5080:Trank1	UTSW	9	111,218,289 (GRCm39)	missense	probably damaging	0.99
R5156:Trank1	UTSW	9	111,219,762 (GRCm39)	missense	probably damaging	1.00
R5174:Trank1	UTSW	9	111,194,627 (GRCm39)	missense	probably benign	0.00
R5234:Trank1	UTSW	9	111,215,535 (GRCm39)	missense	probably damaging	1.00
R5386:Trank1	UTSW	9	111,191,470 (GRCm39)	missense	probably benign	0.12
R5419:Trank1	UTSW	9	111,220,369 (GRCm39)	missense	probably damaging	1.00
R5435:Trank1	UTSW	9	111,220,958 (GRCm39)	missense	probably benign	0.00
R5444:Trank1	UTSW	9	111,222,026 (GRCm39)	missense	probably benign	0.04
R5543:Trank1	UTSW	9	111,195,180 (GRCm39)	missense	probably damaging	0.97
R5560:Trank1	UTSW	9	111,219,635 (GRCm39)	missense	probably damaging	1.00
R5772:Trank1	UTSW	9	111,195,744 (GRCm39)	missense	possibly damaging	0.86
R5774:Trank1	UTSW	9	111,220,294 (GRCm39)	missense	probably damaging	1.00
R5843:Trank1	UTSW	9	111,194,928 (GRCm39)	missense	possibly damaging	0.59
R5858:Trank1	UTSW	9	111,221,604 (GRCm39)	missense	probably benign
R5878:Trank1	UTSW	9	111,195,753 (GRCm39)	missense	possibly damaging	0.93
R5900:Trank1	UTSW	9	111,220,784 (GRCm39)	missense	probably damaging	1.00
R5917:Trank1	UTSW	9	111,191,485 (GRCm39)	missense	probably benign	0.38
R5954:Trank1	UTSW	9	111,194,201 (GRCm39)	missense	probably benign	0.13
R6041:Trank1	UTSW	9	111,206,864 (GRCm39)	missense	possibly damaging	0.94
R6112:Trank1	UTSW	9	111,220,805 (GRCm39)	missense	probably damaging	1.00
R6165:Trank1	UTSW	9	111,220,940 (GRCm39)	missense	probably benign	0.00
R6255:Trank1	UTSW	9	111,181,314 (GRCm39)	critical splice donor site	probably null
R6395:Trank1	UTSW	9	111,196,268 (GRCm39)	missense	probably damaging	1.00
R6567:Trank1	UTSW	9	111,176,589 (GRCm39)	missense	probably benign	0.02
R6644:Trank1	UTSW	9	111,193,902 (GRCm39)	missense	possibly damaging	0.85
R6724:Trank1	UTSW	9	111,194,984 (GRCm39)	missense	probably damaging	1.00
R6788:Trank1	UTSW	9	111,219,747 (GRCm39)	missense	probably damaging	1.00
R6831:Trank1	UTSW	9	111,206,967 (GRCm39)	missense	probably benign	0.00
R6934:Trank1	UTSW	9	111,202,158 (GRCm39)	missense	probably damaging	0.99
R7127:Trank1	UTSW	9	111,194,864 (GRCm39)	missense	possibly damaging	0.85
R7206:Trank1	UTSW	9	111,174,583 (GRCm39)	critical splice donor site	probably null
R7236:Trank1	UTSW	9	111,202,142 (GRCm39)	missense	possibly damaging	0.93
R7247:Trank1	UTSW	9	111,196,580 (GRCm39)	missense	probably damaging	1.00
R7292:Trank1	UTSW	9	111,206,938 (GRCm39)	missense	probably benign	0.02
R7310:Trank1	UTSW	9	111,196,194 (GRCm39)	missense	probably damaging	1.00
R7431:Trank1	UTSW	9	111,191,470 (GRCm39)	missense	probably benign	0.12
R7448:Trank1	UTSW	9	111,195,417 (GRCm39)	missense	probably benign	0.01
R7477:Trank1	UTSW	9	111,194,025 (GRCm39)	missense	probably benign	0.00
R7514:Trank1	UTSW	9	111,193,824 (GRCm39)	missense	probably damaging	1.00
R7595:Trank1	UTSW	9	111,195,059 (GRCm39)	missense	probably damaging	1.00
R7637:Trank1	UTSW	9	111,194,364 (GRCm39)	missense	possibly damaging	0.71
R7648:Trank1	UTSW	9	111,220,753 (GRCm39)	missense	probably benign
R7737:Trank1	UTSW	9	111,195,080 (GRCm39)	nonsense	probably null
R7784:Trank1	UTSW	9	111,193,171 (GRCm39)	missense	probably damaging	1.00
R7884:Trank1	UTSW	9	111,221,584 (GRCm39)	missense	probably benign
R7912:Trank1	UTSW	9	111,220,596 (GRCm39)	missense	probably benign	0.04
R7938:Trank1	UTSW	9	111,194,096 (GRCm39)	missense	probably benign
R7979:Trank1	UTSW	9	111,206,967 (GRCm39)	missense	probably benign	0.00
R8064:Trank1	UTSW	9	111,181,144 (GRCm39)	nonsense	probably null
R8100:Trank1	UTSW	9	111,221,861 (GRCm39)	missense	probably damaging	1.00
R8124:Trank1	UTSW	9	111,207,995 (GRCm39)	missense	probably benign	0.31
R8198:Trank1	UTSW	9	111,219,880 (GRCm39)	missense	probably benign	0.09
R8219:Trank1	UTSW	9	111,193,977 (GRCm39)	missense	probably damaging	1.00
R8223:Trank1	UTSW	9	111,194,957 (GRCm39)	missense	probably damaging	1.00
R8316:Trank1	UTSW	9	111,178,370 (GRCm39)	missense	probably benign	0.38
R8347:Trank1	UTSW	9	111,196,317 (GRCm39)	missense	probably damaging	1.00
R8436:Trank1	UTSW	9	111,220,450 (GRCm39)	missense	possibly damaging	0.86
R8489:Trank1	UTSW	9	111,219,343 (GRCm39)	missense	probably benign	0.01
R8682:Trank1	UTSW	9	111,194,412 (GRCm39)	missense	probably benign	0.01
R8768:Trank1	UTSW	9	111,218,344 (GRCm39)	missense	probably benign	0.00
R8770:Trank1	UTSW	9	111,219,892 (GRCm39)	missense	probably benign	0.00
R8829:Trank1	UTSW	9	111,176,591 (GRCm39)	missense	probably benign
R8838:Trank1	UTSW	9	111,193,973 (GRCm39)	missense	probably benign	0.03
R8855:Trank1	UTSW	9	111,141,289 (GRCm39)	missense	unknown
R8929:Trank1	UTSW	9	111,208,003 (GRCm39)	missense	possibly damaging	0.93
R9047:Trank1	UTSW	9	111,191,500 (GRCm39)	missense	probably damaging	0.99
R9090:Trank1	UTSW	9	111,174,547 (GRCm39)	missense	probably damaging	1.00
R9114:Trank1	UTSW	9	111,162,843 (GRCm39)	missense	probably damaging	1.00
R9133:Trank1	UTSW	9	111,220,770 (GRCm39)	missense	possibly damaging	0.93
R9177:Trank1	UTSW	9	111,221,579 (GRCm39)	missense	probably benign	0.00
R9178:Trank1	UTSW	9	111,196,268 (GRCm39)	missense	probably damaging	1.00
R9271:Trank1	UTSW	9	111,174,547 (GRCm39)	missense	probably damaging	1.00
R9314:Trank1	UTSW	9	111,195,049 (GRCm39)	missense	probably damaging	1.00
R9373:Trank1	UTSW	9	111,194,259 (GRCm39)	missense	probably benign	0.25
R9380:Trank1	UTSW	9	111,221,738 (GRCm39)	missense	probably benign	0.07
R9435:Trank1	UTSW	9	111,193,890 (GRCm39)	missense	probably benign	0.04
R9501:Trank1	UTSW	9	111,176,943 (GRCm39)	missense	probably benign	0.00
R9593:Trank1	UTSW	9	111,191,365 (GRCm39)	missense	probably benign	0.30
R9601:Trank1	UTSW	9	111,202,193 (GRCm39)	missense	probably benign	0.18
R9729:Trank1	UTSW	9	111,220,537 (GRCm39)	missense	probably damaging	1.00
X0064:Trank1	UTSW	9	111,172,304 (GRCm39)	missense	possibly damaging	0.57
Z1088:Trank1	UTSW	9	111,193,778 (GRCm39)	missense	probably damaging	0.99
Z1177:Trank1	UTSW	9	111,221,938 (GRCm39)	missense	possibly damaging	0.47
Z1177:Trank1	UTSW	9	111,196,445 (GRCm39)	missense	possibly damaging	0.83
Z1177:Trank1	UTSW	9	111,140,970 (GRCm39)	missense	unknown

Posted On

2015-04-16