Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00990:Mroh2a'

306778

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Mroh2a

Ensembl Gene

ENSMUSG00000079429

Gene Name

maestro heat-like repeat family member 2A

Synonyms

Heatr7b1, ENSMUSG00000044873, OTTMUSG00000020804

Accession Numbers

Essential gene?

Probably essential (E-score: 0.934) question?

Stock #

IGL00990

Quality Score

Status

Chromosome

Chromosomal Location

88226986-88262289 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 88234120 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Aspartic acid at position 309 (G309D)

Ref Sequence

ENSEMBL: ENSMUSP00000108755 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000061013] [ENSMUST00000113130]

AlphaFold

D3Z750

Predicted Effect

probably benign
Transcript: ENSMUST00000061013

SMART Domains

Protein: ENSMUSP00000130508
Gene: ENSMUSG00000079429

Domain	Start	End	E-Value	Type
low complexity region	9	26	N/A	INTRINSIC
low complexity region	99	112	N/A	INTRINSIC
low complexity region	1235	1248	N/A	INTRINSIC
SCOP:d1jdha_	1371	1669	9e-8	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000113130
AA Change: G309D

PolyPhen 2 Score 0.762 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000108755
Gene: ENSMUSG00000079429
AA Change: G309D

Domain	Start	End	E-Value	Type
low complexity region	9	26	N/A	INTRINSIC
low complexity region	99	112	N/A	INTRINSIC
low complexity region	1232	1245	N/A	INTRINSIC
SCOP:d1gw5a_	1446	1671	6e-6	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142632

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000148474

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a HEAT-domain-containing protein. The function of the encoded protein has not been characterized. [provided by RefSeq, Aug 2016]

Allele List at MGI

Other mutations in this stock

Total: 148 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
6430531B16Rik	A	C	7: 139,978,103	V60G	probably damaging	Het
Adcy8	C	A	15: 64,822,313	V372L	probably benign	Het
Bod1l	T	C	5: 41,828,865	D458G	probably benign	Het
C87414	T	A	5: 93,636,477	Q376L	probably damaging	Het
Cacna1c	G	T	6: 118,613,295	H1416N	probably damaging	Het
Cacna2d1	T	C	5: 15,935,069	I19T	probably benign	Het
Cadps	T	A	14: 12,715,374	T153S	possibly damaging	Het
Cd200r1	A	T	16: 44,794,309	D317V	possibly damaging	Het
Dcaf5	C	T	12: 80,338,832	R840H	probably benign	Het
Dnhd1	A	C	7: 105,721,688	H4725P	possibly damaging	Het
Echdc3	C	A	2: 6,195,727	L149F	probably benign	Het
Efhb	T	G	17: 53,462,621	Q220P	possibly damaging	Het
Efr3b	A	T	12: 3,975,411	Y18*	probably null	Het
Eri1	T	C	8: 35,482,682	K41R	possibly damaging	Het
Eri1	C	A	8: 35,482,646	G53V	probably benign	Het
Gm10212	A	G	19: 11,569,560		noncoding transcript	Het
Gm11168	T	G	9: 3,005,124	F201C	probably damaging	Het
Gm14412	A	C	2: 177,315,686	S139A	probably benign	Het
Gm21411	C	T	4: 146,892,610	S69N	possibly damaging	Het
Gm21671	A	C	5: 25,954,224	W41G	probably benign	Het
Gm21738	A	G	14: 19,418,885	C16R	probably benign	Het
Gm21967	T	A	13: 119,609,535		probably benign	Het
Gm4952	A	T	19: 12,623,623	D69V	probably damaging	Het
Gm5591	T	G	7: 38,520,414	K345T	probably benign	Het
Gm7647	T	C	5: 94,962,980	S7P	probably benign	Het
Gm9733	C	T	3: 15,332,145		probably null	Het
Gm9758	G	A	5: 14,913,508		probably benign	Het
Gtse1	C	A	15: 85,868,817	Q378K	possibly damaging	Het
Haus3	T	C	5: 34,166,346	K307E	probably benign	Het
Hjurp	A	G	1: 88,270,269	L96S	probably benign	Het
Ifi205	T	A	1: 174,027,333		probably benign	Het
Ighg1	A	G	12: 113,329,184	V255A	unknown	Het
Ighv14-4	T	A	12: 114,176,632	M49L	probably benign	Het
Jak1	A	C	4: 101,171,357	L508R	probably damaging	Het
Kif18a	A	G	2: 109,334,422	Q821R	probably benign	Het
Kif21b	T	C	1: 136,152,342	S539P	possibly damaging	Het
Klhdc2	T	C	12: 69,307,213	V266A	probably benign	Het
Lonp2	G	T	8: 86,641,533		probably benign	Het
Mpdz	C	T	4: 81,303,584		probably benign	Het
Mtif3	C	A	5: 146,959,104	G58*	probably null	Het
Muc4	C	A	16: 32,753,955	T1277K	possibly damaging	Het
Muc4	C	T	16: 32,755,805		probably benign	Het
Muc4	C	T	16: 32,753,823	P1233L	probably benign	Het
Muc4	G	T	16: 32,753,848	K1241N	probably benign	Het
Muc4	G	A	16: 32,753,849	G1242R	probably benign	Het
Muc4	T	G	16: 32,753,863	N1246K	probably benign	Het
Muc4	A	G	16: 32,754,071	R1316G	probably benign	Het
Muc4	C	T	16: 32,752,569	P816S	probably benign	Het
Muc4	A	T	16: 32,753,886	E1254V	probably benign	Het
Muc6	C	T	7: 141,638,890	A1957T	possibly damaging	Het
Naca	T	A	10: 128,043,800		probably benign	Het
Nars2	A	T	7: 97,002,790		probably benign	Het
Odf3l1	T	C	9: 56,849,057	E225G	probably benign	Het
Olfr1445	G	T	19: 12,883,901	V7L	probably benign	Het
Olfr342	A	C	2: 36,527,993	I194L	probably benign	Het
Olfr549	G	T	7: 102,554,891	L202F	probably damaging	Het
Olfr812	T	C	10: 129,842,473	T190A	probably damaging	Het
Pcdh7	G	A	5: 57,720,464	E454K	possibly damaging	Het
Pip5kl1	C	A	2: 32,583,347	A332D	probably benign	Het
Pisd	A	T	5: 32,739,358	S280T	probably benign	Het
Pramel5	A	G	4: 144,273,979	L9P	probably damaging	Het
Prkd3	G	T	17: 78,954,523	N787K	probably benign	Het
Prkdc	A	T	16: 15,702,115	H1139L	probably benign	Het
R3hdm1	A	G	1: 128,162,196		probably benign	Het
Rbfox2	T	C	15: 77,102,936	N206D	probably damaging	Het
Rlf	T	C	4: 121,148,339	E1258G	possibly damaging	Het
Rpl8	T	C	15: 76,905,042		probably benign	Het
Senp5	A	C	16: 31,990,274	V27G	probably benign	Het
Serpina1b	T	A	12: 103,728,266	K406N	probably damaging	Het
Sfi1	G	A	11: 3,134,337	A975V	probably benign	Het
Sfi1	T	C	11: 3,143,689		probably benign	Het
Sfi1	C	T	11: 3,135,671	A853T	probably damaging	Het
Shc1	T	C	3: 89,424,229	S154P	probably damaging	Het
Skint5	A	G	4: 113,542,873		probably null	Het
Slc17a8	T	C	10: 89,576,530	D531G	probably benign	Het
Slc4a10	A	C	2: 62,286,940	T718P	probably damaging	Het
Slc7a11	C	T	3: 50,379,069	R411Q	probably damaging	Het
Slitrk3	A	G	3: 73,050,081	F453L	probably damaging	Het
Slk	A	C	19: 47,580,252	Q20P	probably damaging	Het
Smg5	T	C	3: 88,343,038		probably null	Het
Sp110	G	A	1: 85,586,281	R252C	possibly damaging	Het
Sp140	C	T	1: 85,626,165	R242C	possibly damaging	Het
Sp140	G	A	1: 85,626,133	R231K	probably benign	Het
Speer4b	G	A	5: 27,501,274	P30S	probably damaging	Het
Stim1	T	A	7: 102,426,747	H395Q	probably damaging	Het
Sult2a1	T	C	7: 13,804,036	I187M	probably benign	Het
Thap1	G	A	8: 26,162,731	D189N	probably benign	Het
Thap1	C	T	8: 26,160,882	P37L	possibly damaging	Het
Thrap3	C	T	4: 126,165,395		probably benign	Het
Tmem132d	C	T	5: 127,784,832	V742I	possibly damaging	Het
Tmprss9	A	G	10: 80,892,292	D572G	possibly damaging	Het
Tmtc1	T	G	6: 148,443,944	T86P	probably benign	Het
Trip12	A	T	1: 84,751,884	N1026K	probably damaging	Het
Ttll5	T	A	12: 85,876,589	V280E	probably damaging	Het
Ubn2	T	A	6: 38,482,605	D592E	possibly damaging	Het
Ubr1	T	G	2: 120,930,872	H608P	probably damaging	Het
Ugt1a6b	A	T	1: 88,215,178		probably null	Het
Vmn1r77	C	A	7: 12,041,768	S89Y	probably benign	Het
Vmn1r77	A	C	7: 12,041,476	I60L	probably benign	Het
Vmn2r114	A	T	17: 23,291,238	L756Q	probably damaging	Het
Vmn2r114	G	A	17: 23,290,965	A847V	probably benign	Het
Vmn2r114	G	T	17: 23,290,983	S841Y	probably benign	Het
Vmn2r115	C	T	17: 23,346,264	S375F	probably benign	Het
Vmn2r115	G	A	17: 23,359,779	G742D	probably damaging	Het
Vmn2r115	G	T	17: 23,348,034	G507*	probably null	Het
Vmn2r115	T	A	17: 23,359,824	L757Q	probably damaging	Het
Vmn2r115	A	G	17: 23,356,960	M511V	probably benign	Het
Vmn2r115	C	T	17: 23,346,371	Q411*	probably null	Het
Vmn2r115	A	G	17: 23,346,372	Q411R	probably benign	Het
Vmn2r115	C	T	17: 23,359,397	P615S	probably damaging	Het
Vmn2r115	G	A	17: 23,346,278	E380K	probably benign	Het
Vmn2r115	A	G	17: 23,346,161	N341D	probably benign	Het
Vmn2r115	G	T	17: 23,359,349	A599S	probably benign	Het
Vmn2r115	A	C	17: 23,346,339	N400T	probably damaging	Het
Vmn2r115	C	T	17: 23,346,176	P346S	probably benign	Het
Vmn2r115	A	T	17: 23,346,206	M356L	possibly damaging	Het
Vmn2r116	C	T	17: 23,397,727	P540S	probably damaging	Het
Vmn2r116	C	T	17: 23,387,236	S374F	probably benign	Het
Vmn2r117	C	T	17: 23,477,840	A198T	probably damaging	Het
Vmn2r117	T	G	17: 23,475,429	K481N	probably damaging	Het
Vmn2r117	A	C	17: 23,479,546	S18A	probably benign	Het
Vmn2r121	T	G	X: 124,127,802	K840N	probably benign	Het
Vmn2r121	C	T	X: 124,133,716	E73K	probably benign	Het
Vmn2r121	T	A	X: 124,127,783	N847Y	possibly damaging	Het
Vmn2r125	C	T	4: 156,351,038	T237I	probably benign	Het
Vmn2r125	A	T	4: 156,351,037	T237S	probably benign	Het
Vmn2r125	A	C	4: 156,350,900	Q191P	probably benign	Het
Vmn2r125	C	A	4: 156,350,899	Q191K	probably benign	Het
Vmn2r125	T	C	4: 156,350,966	V213A	probably benign	Het
Vmn2r125	T	C	4: 156,351,383	M352T	probably benign	Het
Vmn2r125	T	A	4: 156,351,226	L300M	probably benign	Het
Vmn2r88	A	G	14: 51,413,125	I98M	probably benign	Het
Vmn2r88	T	C	14: 51,413,060	F77L	probably benign	Het
Vmn2r88	T	C	14: 51,413,256	I142T	probably benign	Het
Vmn2r88	C	T	14: 51,416,802	P539L	possibly damaging	Het
Vmn2r89	T	G	14: 51,457,493	L477V	probably benign	Het
Vmn2r89	A	C	14: 51,455,971	Q259H	probably benign	Het
Vmn2r-ps159	T	C	4: 156,334,263		noncoding transcript	Het
Vmn2r-ps159	C	A	4: 156,338,435		noncoding transcript	Het
Vmn2r-ps159	G	T	4: 156,338,460		noncoding transcript	Het
Vmn2r-ps159	T	G	4: 156,338,484		noncoding transcript	Het
Vmn2r-ps159	G	T	4: 156,334,397		noncoding transcript	Het
Vmn2r-ps159	T	G	4: 156,334,562		noncoding transcript	Het
Vmn2r-ps159	A	T	4: 156,338,146		noncoding transcript	Het
Zfp180	G	A	7: 24,104,416	C85Y	possibly damaging	Het
Zfp180	C	T	7: 24,104,830	R225C	probably benign	Het
Zfp180	G	A	7: 24,104,995	V280M	possibly damaging	Het
Zfp982	G	A	4: 147,512,369	C61Y	probably benign	Het

Other mutations in Mroh2a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00990:Mroh2a	APN	1	88230746	missense	probably damaging	0.99
IGL00990:Mroh2a	APN	1	88244970	missense	probably benign	0.03
IGL03097:Mroh2a	UTSW	1	88235376	missense	probably benign	0.30
R0032:Mroh2a	UTSW	1	88256166	frame shift	probably null
R0068:Mroh2a	UTSW	1	88256166	frame shift	probably null
R0139:Mroh2a	UTSW	1	88257802	missense	probably damaging	1.00
R0197:Mroh2a	UTSW	1	88246042	missense	probably damaging	1.00
R0242:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R0322:Mroh2a	UTSW	1	88230680	nonsense	probably null
R0374:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R0387:Mroh2a	UTSW	1	88246042	missense	probably damaging	1.00
R0412:Mroh2a	UTSW	1	88235216	missense	probably benign	0.01
R0536:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R0548:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R0580:Mroh2a	UTSW	1	88243950	missense	probably damaging	1.00
R0581:Mroh2a	UTSW	1	88256166	frame shift	probably null
R0583:Mroh2a	UTSW	1	88256166	frame shift	probably null
R0613:Mroh2a	UTSW	1	88243950	missense	probably damaging	1.00
R0652:Mroh2a	UTSW	1	88230680	nonsense	probably null
R0657:Mroh2a	UTSW	1	88255565	missense	probably damaging	1.00
R0659:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R0659:Mroh2a	UTSW	1	88250342	missense	probably damaging	1.00
R0671:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R0675:Mroh2a	UTSW	1	88228380	missense	probably damaging	0.99
R0675:Mroh2a	UTSW	1	88250342	missense	probably damaging	1.00
R0689:Mroh2a	UTSW	1	88230680	nonsense	probably null
R0689:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R0735:Mroh2a	UTSW	1	88243950	missense	probably damaging	1.00
R0761:Mroh2a	UTSW	1	88243950	missense	probably damaging	1.00
R0766:Mroh2a	UTSW	1	88230680	nonsense	probably null
R0845:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R0853:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R0959:Mroh2a	UTSW	1	88232257	frame shift	probably null
R0960:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R1004:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R1013:Mroh2a	UTSW	1	88234612	critical splice donor site	probably null
R1028:Mroh2a	UTSW	1	88235376	missense	probably benign	0.30
R1268:Mroh2a	UTSW	1	88230680	nonsense	probably null
R1281:Mroh2a	UTSW	1	88256167	frame shift	probably null
R1414:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R1439:Mroh2a	UTSW	1	88257802	missense	probably damaging	1.00
R1441:Mroh2a	UTSW	1	88241631	missense	possibly damaging	0.93
R1442:Mroh2a	UTSW	1	88232353	splice site	probably benign
R1442:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R1465:Mroh2a	UTSW	1	88257802	missense	probably damaging	1.00
R1662:Mroh2a	UTSW	1	88241618	missense	probably benign	0.07
R1686:Mroh2a	UTSW	1	88230680	nonsense	probably null
R1686:Mroh2a	UTSW	1	88234612	critical splice donor site	probably null
R1780:Mroh2a	UTSW	1	88230680	nonsense	probably null
R1846:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R1899:Mroh2a	UTSW	1	88235376	missense	probably benign	0.30
R1958:Mroh2a	UTSW	1	88237491	nonsense	probably null
R2122:Mroh2a	UTSW	1	88256754	missense	probably benign	0.37
R2248:Mroh2a	UTSW	1	88256754	missense	probably benign	0.37
R2306:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R2869:Mroh2a	UTSW	1	88232257	frame shift	probably null
R2870:Mroh2a	UTSW	1	88232257	frame shift	probably null
R2871:Mroh2a	UTSW	1	88255565	missense	probably damaging	1.00
R2872:Mroh2a	UTSW	1	88232257	frame shift	probably null
R3408:Mroh2a	UTSW	1	88232257	frame shift	probably null
R3608:Mroh2a	UTSW	1	88244995	missense	probably damaging	1.00
R3730:Mroh2a	UTSW	1	88232257	frame shift	probably null
R3937:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R4022:Mroh2a	UTSW	1	88246042	missense	probably damaging	1.00
R4049:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R4133:Mroh2a	UTSW	1	88254965	missense	possibly damaging	0.95
R4361:Mroh2a	UTSW	1	88254965	missense	possibly damaging	0.95
R4392:Mroh2a	UTSW	1	88259589	missense	probably damaging	1.00
R4401:Mroh2a	UTSW	1	88254935	missense	possibly damaging	0.72
R4402:Mroh2a	UTSW	1	88254935	missense	possibly damaging	0.72
R4575:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R4625:Mroh2a	UTSW	1	88254965	missense	possibly damaging	0.95
R4631:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R4665:Mroh2a	UTSW	1	88241618	missense	probably benign	0.07
R4701:Mroh2a	UTSW	1	88234612	critical splice donor site	probably null
R4701:Mroh2a	UTSW	1	88241618	missense	probably benign	0.07
R4771:Mroh2a	UTSW	1	88251365	missense	probably damaging	1.00
R4795:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R4839:Mroh2a	UTSW	1	88237944	missense	probably damaging	1.00
R4873:Mroh2a	UTSW	1	88254935	missense	possibly damaging	0.72
R4875:Mroh2a	UTSW	1	88254935	missense	possibly damaging	0.72
R4896:Mroh2a	UTSW	1	88256754	missense	probably benign	0.37
R5007:Mroh2a	UTSW	1	88232257	frame shift	probably null
R5031:Mroh2a	UTSW	1	88232257	frame shift	probably null
R5062:Mroh2a	UTSW	1	88232257	frame shift	probably null
R5301:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R5367:Mroh2a	UTSW	1	88254965	missense	possibly damaging	0.95
R5371:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R5446:Mroh2a	UTSW	1	88254965	missense	possibly damaging	0.95
R5484:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R5506:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R5561:Mroh2a	UTSW	1	88232257	frame shift	probably null
R5615:Mroh2a	UTSW	1	88232257	frame shift	probably null
R5825:Mroh2a	UTSW	1	88230680	nonsense	probably null
R5891:Mroh2a	UTSW	1	88241615	missense	possibly damaging	0.93
R5906:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R5928:Mroh2a	UTSW	1	88241618	missense	probably benign	0.07
R6004:Mroh2a	UTSW	1	88248655	missense	probably damaging	1.00
R6035:Mroh2a	UTSW	1	88230668	missense	probably damaging	1.00
R6064:Mroh2a	UTSW	1	88232257	frame shift	probably null
R6074:Mroh2a	UTSW	1	88258664	missense	probably benign	0.00
R6091:Mroh2a	UTSW	1	88232257	frame shift	probably null
R6127:Mroh2a	UTSW	1	88234612	critical splice donor site	probably null
R6234:Mroh2a	UTSW	1	88234612	critical splice donor site	probably null
R6234:Mroh2a	UTSW	1	88256754	missense	probably benign	0.37
R6244:Mroh2a	UTSW	1	88256754	missense	probably benign	0.37
R6464:Mroh2a	UTSW	1	88257802	missense	probably damaging	1.00
R6465:Mroh2a	UTSW	1	88232257	frame shift	probably null
R6575:Mroh2a	UTSW	1	88232257	frame shift	probably null
R6809:Mroh2a	UTSW	1	88235216	missense	probably benign	0.01
R6819:Mroh2a	UTSW	1	88242420	missense	possibly damaging	0.77
R6854:Mroh2a	UTSW	1	88243950	missense	probably damaging	1.00
R6860:Mroh2a	UTSW	1	88254935	missense	possibly damaging	0.72
R7126:Mroh2a	UTSW	1	88254935	missense	possibly damaging	0.72
R7818:Mroh2a	UTSW	1	88234612	critical splice donor site	probably null
R8350:Mroh2a	UTSW	1	88244083	splice site	probably null
R9414:Mroh2a	UTSW	1	88251374	missense	probably benign	0.26
RF024:Mroh2a	UTSW	1	88242485	missense	probably damaging	1.00
V5622:Mroh2a	UTSW	1	88227091	start gained	probably benign
V8831:Mroh2a	UTSW	1	88256167	frame shift	probably null
X0027:Mroh2a	UTSW	1	88248613	missense	possibly damaging	0.86
X0028:Mroh2a	UTSW	1	88232257	frame shift	probably null
X0028:Mroh2a	UTSW	1	88256166	frame shift	probably null
X0033:Mroh2a	UTSW	1	88256166	frame shift	probably null
X0034:Mroh2a	UTSW	1	88232257	frame shift	probably null
X0034:Mroh2a	UTSW	1	88232292	missense	probably damaging	1.00
X0034:Mroh2a	UTSW	1	88256166	frame shift	probably null
X0039:Mroh2a	UTSW	1	88232257	frame shift	probably null
X0057:Mroh2a	UTSW	1	88232257	frame shift	probably null
X0057:Mroh2a	UTSW	1	88255655	missense	probably benign	0.25
X0057:Mroh2a	UTSW	1	88256166	frame shift	probably null
X0063:Mroh2a	UTSW	1	88232257	frame shift	probably null
Z1188:Mroh2a	UTSW	1	88235216	missense	probably benign	0.01
Z1190:Mroh2a	UTSW	1	88232257	frame shift	probably null
Z1192:Mroh2a	UTSW	1	88235216	missense	probably benign	0.01

Posted On

2015-04-16