Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03177:Dhx30'

412026

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Dhx30

Ensembl Gene

ENSMUSG00000032480

Gene Name

DExH-box helicase 30

Synonyms

2810477H02Rik, helG, C130058C04Rik, Ddx30, DEAH (Asp-Glu-Ala-His) box polypeptide 30

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL03177

Quality Score

Status

Chromosome

Chromosomal Location

109913387-109946728 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 109917078 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 479 (H479R)

Ref Sequence

ENSEMBL: ENSMUSP00000062622 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035055] [ENSMUST00000062368] [ENSMUST00000111991] [ENSMUST00000163979] [ENSMUST00000164930] [ENSMUST00000165596] [ENSMUST00000165876] [ENSMUST00000198425] [ENSMUST00000196171] [ENSMUST00000199529] [ENSMUST00000200066] [ENSMUST00000197928] [ENSMUST00000198443] [ENSMUST00000199693] [ENSMUST00000199498]

AlphaFold

Q99PU8

Predicted Effect

probably benign
Transcript: ENSMUST00000035055

SMART Domains

Protein: ENSMUSP00000035055
Gene: ENSMUSG00000032479

Domain	Start	End	E-Value	Type
low complexity region	254	265	N/A	INTRINSIC
internal_repeat_1	266	379	4.96e-7	PROSPERO
low complexity region	401	420	N/A	INTRINSIC
internal_repeat_1	439	550	4.96e-7	PROSPERO
low complexity region	659	674	N/A	INTRINSIC
low complexity region	720	742	N/A	INTRINSIC
low complexity region	760	775	N/A	INTRINSIC
low complexity region	879	889	N/A	INTRINSIC
Pfam:Tubulin-binding	903	926	2e-12	PFAM
Pfam:Tubulin-binding	965	995	4.9e-18	PFAM
Pfam:Tubulin-binding	996	1026	7.4e-18	PFAM
Pfam:Tubulin-binding	1027	1058	4.4e-15	PFAM
low complexity region	1093	1108	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000062368
AA Change: H479R

PolyPhen 2 Score 0.752 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000062622
Gene: ENSMUSG00000032480
AA Change: H479R

Domain	Start	End	E-Value	Type
low complexity region	1	12	N/A	INTRINSIC
low complexity region	48	64	N/A	INTRINSIC
internal_repeat_1	76	123	2.53e-5	PROSPERO
low complexity region	217	228	N/A	INTRINSIC
internal_repeat_1	268	314	2.53e-5	PROSPERO
low complexity region	321	342	N/A	INTRINSIC
DEXDc	461	650	9.66e-29	SMART
low complexity region	679	689	N/A	INTRINSIC
HELICc	711	816	1.63e-17	SMART
HA2	879	969	5.16e-22	SMART
Pfam:OB_NTP_bind	984	1134	5.7e-9	PFAM
low complexity region	1200	1208	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000111991
AA Change: H450R

PolyPhen 2 Score 0.681 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000107622
Gene: ENSMUSG00000032480
AA Change: H450R

Domain	Start	End	E-Value	Type
internal_repeat_1	47	94	6.21e-5	PROSPERO
low complexity region	188	199	N/A	INTRINSIC
internal_repeat_1	239	285	6.21e-5	PROSPERO
low complexity region	292	313	N/A	INTRINSIC
DEXDc	432	621	9.66e-29	SMART
low complexity region	650	660	N/A	INTRINSIC
HELICc	682	787	1.63e-17	SMART
HA2	850	940	5.16e-22	SMART
Pfam:OB_NTP_bind	952	1106	2.1e-7	PFAM
low complexity region	1171	1179	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000163979

SMART Domains

Protein: ENSMUSP00000129362
Gene: ENSMUSG00000032479

Domain	Start	End	E-Value	Type
low complexity region	9	17	N/A	INTRINSIC
low complexity region	324	341	N/A	INTRINSIC
low complexity region	365	376	N/A	INTRINSIC
low complexity region	506	521	N/A	INTRINSIC
low complexity region	567	589	N/A	INTRINSIC
low complexity region	607	622	N/A	INTRINSIC
low complexity region	726	736	N/A	INTRINSIC
Pfam:Tubulin-binding	743	773	5.8e-16	PFAM
Pfam:Tubulin-binding	774	804	2.2e-18	PFAM
Pfam:Tubulin-binding	805	836	1.6e-11	PFAM
low complexity region	871	886	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000164930

SMART Domains

Protein: ENSMUSP00000131285
Gene: ENSMUSG00000032479

Domain	Start	End	E-Value	Type
low complexity region	9	17	N/A	INTRINSIC
low complexity region	324	341	N/A	INTRINSIC
low complexity region	365	376	N/A	INTRINSIC
low complexity region	506	521	N/A	INTRINSIC
low complexity region	567	589	N/A	INTRINSIC
low complexity region	607	622	N/A	INTRINSIC
low complexity region	726	736	N/A	INTRINSIC
Pfam:Tubulin-binding	743	773	6e-16	PFAM
Pfam:Tubulin-binding	774	804	4.5e-19	PFAM
Pfam:Tubulin-binding	805	835	2.3e-18	PFAM
Pfam:Tubulin-binding	836	867	1.6e-11	PFAM
low complexity region	902	917	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000165596
AA Change: H473R

PolyPhen 2 Score 0.681 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000129174
Gene: ENSMUSG00000032480
AA Change: H473R

Domain	Start	End	E-Value	Type
internal_repeat_1	70	117	6.77e-5	PROSPERO
low complexity region	211	222	N/A	INTRINSIC
internal_repeat_1	262	308	6.77e-5	PROSPERO
low complexity region	315	336	N/A	INTRINSIC
DEXDc	455	644	9.66e-29	SMART
low complexity region	673	683	N/A	INTRINSIC
HELICc	705	810	1.63e-17	SMART
HA2	873	963	5.16e-22	SMART
Pfam:OB_NTP_bind	975	1129	1.8e-7	PFAM
low complexity region	1194	1202	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000165876

SMART Domains

Protein: ENSMUSP00000132662
Gene: ENSMUSG00000032479

Domain	Start	End	E-Value	Type
low complexity region	254	265	N/A	INTRINSIC
internal_repeat_1	266	379	4.95e-7	PROSPERO
low complexity region	401	420	N/A	INTRINSIC
internal_repeat_1	439	550	4.95e-7	PROSPERO
low complexity region	659	674	N/A	INTRINSIC
low complexity region	720	742	N/A	INTRINSIC
low complexity region	760	775	N/A	INTRINSIC
low complexity region	879	889	N/A	INTRINSIC
Pfam:Tubulin-binding	896	926	8.5e-16	PFAM
Pfam:Tubulin-binding	965	995	6.4e-19	PFAM
Pfam:Tubulin-binding	996	1026	3.3e-18	PFAM
Pfam:Tubulin-binding	1027	1058	2.3e-11	PFAM
low complexity region	1093	1108	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000198425
AA Change: H473R

PolyPhen 2 Score 0.681 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000142659
Gene: ENSMUSG00000032480
AA Change: H473R

Domain	Start	End	E-Value	Type
internal_repeat_1	70	117	6.77e-5	PROSPERO
low complexity region	211	222	N/A	INTRINSIC
internal_repeat_1	262	308	6.77e-5	PROSPERO
low complexity region	315	336	N/A	INTRINSIC
DEXDc	455	644	9.66e-29	SMART
low complexity region	673	683	N/A	INTRINSIC
HELICc	705	810	1.63e-17	SMART
HA2	873	963	5.16e-22	SMART
Pfam:OB_NTP_bind	975	1129	1.8e-7	PFAM
low complexity region	1194	1202	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000196171
AA Change: H442R

PolyPhen 2 Score 0.555 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000143616
Gene: ENSMUSG00000032480
AA Change: H442R

Domain	Start	End	E-Value	Type
internal_repeat_1	39	86	5.84e-5	PROSPERO
low complexity region	180	191	N/A	INTRINSIC
internal_repeat_1	231	277	5.84e-5	PROSPERO
low complexity region	284	305	N/A	INTRINSIC
DEXDc	424	613	9.66e-29	SMART
low complexity region	642	652	N/A	INTRINSIC
HELICc	674	779	1.63e-17	SMART
HA2	842	932	5.16e-22	SMART
Pfam:OB_NTP_bind	947	1097	2.8e-9	PFAM
low complexity region	1163	1171	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000199529
AA Change: H450R

PolyPhen 2 Score 0.681 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000142489
Gene: ENSMUSG00000032480
AA Change: H450R

Domain	Start	End	E-Value	Type
internal_repeat_1	47	94	6.21e-5	PROSPERO
low complexity region	188	199	N/A	INTRINSIC
internal_repeat_1	239	285	6.21e-5	PROSPERO
low complexity region	292	313	N/A	INTRINSIC
DEXDc	432	621	9.66e-29	SMART
low complexity region	650	660	N/A	INTRINSIC
HELICc	682	787	1.63e-17	SMART
HA2	850	940	5.16e-22	SMART
Pfam:OB_NTP_bind	952	1106	2.1e-7	PFAM
low complexity region	1171	1179	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000200066
AA Change: H450R

PolyPhen 2 Score 0.681 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000143371
Gene: ENSMUSG00000032480
AA Change: H450R

Domain	Start	End	E-Value	Type
internal_repeat_1	47	94	6.21e-5	PROSPERO
low complexity region	188	199	N/A	INTRINSIC
internal_repeat_1	239	285	6.21e-5	PROSPERO
low complexity region	292	313	N/A	INTRINSIC
DEXDc	432	621	9.66e-29	SMART
low complexity region	650	660	N/A	INTRINSIC
HELICc	682	787	1.63e-17	SMART
HA2	850	940	5.16e-22	SMART
Pfam:OB_NTP_bind	952	1106	2.1e-7	PFAM
low complexity region	1171	1179	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000197928
AA Change: H450R

PolyPhen 2 Score 0.681 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000142549
Gene: ENSMUSG00000032480
AA Change: H450R

Domain	Start	End	E-Value	Type
internal_repeat_1	47	94	6.21e-5	PROSPERO
low complexity region	188	199	N/A	INTRINSIC
internal_repeat_1	239	285	6.21e-5	PROSPERO
low complexity region	292	313	N/A	INTRINSIC
DEXDc	432	621	9.66e-29	SMART
low complexity region	650	660	N/A	INTRINSIC
HELICc	682	787	1.63e-17	SMART
HA2	850	940	5.16e-22	SMART
Pfam:OB_NTP_bind	952	1106	2.1e-7	PFAM
low complexity region	1171	1179	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198026

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196914

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200029

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196182

Predicted Effect

probably benign
Transcript: ENSMUST00000198443

SMART Domains

Protein: ENSMUSP00000142836
Gene: ENSMUSG00000032480

Domain	Start	End	E-Value	Type
low complexity region	1	12	N/A	INTRINSIC
low complexity region	48	64	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000199332

Predicted Effect

probably benign
Transcript: ENSMUST00000199693

Predicted Effect

probably benign
Transcript: ENSMUST00000200593

Predicted Effect

probably benign
Transcript: ENSMUST00000199498

SMART Domains

Protein: ENSMUSP00000142439
Gene: ENSMUSG00000032479

Domain	Start	End	E-Value	Type
low complexity region	9	17	N/A	INTRINSIC
low complexity region	324	341	N/A	INTRINSIC
low complexity region	365	376	N/A	INTRINSIC
low complexity region	506	521	N/A	INTRINSIC
low complexity region	567	589	N/A	INTRINSIC
low complexity region	607	622	N/A	INTRINSIC
low complexity region	726	736	N/A	INTRINSIC
Pfam:Tubulin-binding	743	773	5.8e-16	PFAM
Pfam:Tubulin-binding	774	804	2.2e-18	PFAM
Pfam:Tubulin-binding	805	836	1.6e-11	PFAM
low complexity region	871	886	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The family member encoded by this gene is a mitochondrial nucleoid protein that associates with mitochondrial DNA. It has also been identified as a component of a transcriptional repressor complex that functions in retinal development, and it is required to optimize the function of the zinc-finger antiviral protein. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit complete embryonic lethality associated with embryonic growth retardation, failure of initiation of embryo turning, and absence of organized somites and neural tube formation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrg2	T	C	X: 159,221,259 (GRCm39)	I23T	possibly damaging	Het
Ank2	C	A	3: 126,749,519 (GRCm39)	E503D	probably damaging	Het
Anxa7	T	C	14: 20,506,654 (GRCm39)	I451V	probably benign	Het
Capn10	T	C	1: 92,862,704 (GRCm39)	F37L	probably benign	Het
Cyp4f13	A	G	17: 33,165,888 (GRCm39)	I30T	possibly damaging	Het
Ddx27	A	G	2: 166,869,840 (GRCm39)	N392D	possibly damaging	Het
Dnah5	A	G	15: 28,295,545 (GRCm39)	Y1426C	probably damaging	Het
Dnajc2	A	G	5: 21,980,079 (GRCm39)		probably benign	Het
Fbxw8	C	A	5: 118,267,045 (GRCm39)		probably benign	Het
Grik5	G	A	7: 24,714,879 (GRCm39)	T705I	probably damaging	Het
H2ac4	T	A	13: 23,935,509 (GRCm39)		probably benign	Het
H2-M3	G	T	17: 37,581,207 (GRCm39)	V19F	possibly damaging	Het
Hapln2	C	A	3: 87,930,078 (GRCm39)	C266F	probably damaging	Het
Hspbp1	A	T	7: 4,667,700 (GRCm39)		probably null	Het
Jak3	T	A	8: 72,135,014 (GRCm39)	V549D	probably damaging	Het
Mark1	A	G	1: 184,677,104 (GRCm39)	S49P	probably damaging	Het
Mdfic	T	C	6: 15,770,450 (GRCm39)	V152A	probably damaging	Het
Mgat4a	C	A	1: 37,483,968 (GRCm39)	V501L	probably damaging	Het
Mlxip	C	A	5: 123,584,044 (GRCm39)	P536T	possibly damaging	Het
Mrpl2	A	T	17: 46,959,963 (GRCm39)	T213S	probably damaging	Het
Nos1ap	C	A	1: 170,218,299 (GRCm39)		probably null	Het
Or4a74	C	T	2: 89,439,826 (GRCm39)	V207I	probably benign	Het
Or6c1b	T	C	10: 129,272,684 (GRCm39)	M1T	probably null	Het
Or8b50	T	A	9: 38,517,867 (GRCm39)	Y35*	probably null	Het
P2rx2	T	C	5: 110,489,479 (GRCm39)	I251V	probably damaging	Het
Parva	T	A	7: 112,172,140 (GRCm39)		probably benign	Het
Phf10	G	A	17: 15,166,493 (GRCm39)	T459I	probably damaging	Het
Prg4	T	A	1: 150,331,354 (GRCm39)		probably benign	Het
Pum3	A	T	19: 27,367,612 (GRCm39)	I639N	probably benign	Het
Rlf	T	A	4: 121,005,276 (GRCm39)	K1235*	probably null	Het
Ryr3	T	A	2: 112,859,016 (GRCm39)	I46F	probably benign	Het
Sall3	A	G	18: 81,016,183 (GRCm39)	S582P	probably benign	Het
Scn3b	A	C	9: 40,181,338 (GRCm39)	Y17S	probably benign	Het
Senp8	A	G	9: 59,644,611 (GRCm39)	C169R	probably damaging	Het
Sgsm1	C	T	5: 113,398,859 (GRCm39)	A1025T	probably damaging	Het
Six1	T	C	12: 73,090,514 (GRCm39)	E217G	possibly damaging	Het
Slc38a8	T	C	8: 120,212,251 (GRCm39)	D364G	probably damaging	Het
Stk10	A	T	11: 32,564,592 (GRCm39)	E801V	probably damaging	Het
Ston2	A	T	12: 91,614,431 (GRCm39)	I659N	probably damaging	Het
Stxbp4	T	C	11: 90,462,579 (GRCm39)	Q331R	probably benign	Het
Synpo2	A	T	3: 122,914,864 (GRCm39)	V54E	probably damaging	Het
Tax1bp1	A	G	6: 52,713,932 (GRCm39)	D237G	possibly damaging	Het
Tmigd1	T	C	11: 76,797,774 (GRCm39)	Y39H	probably benign	Het
Vmn1r15	A	G	6: 57,235,458 (GRCm39)	T109A	probably benign	Het
Vmn1r209	T	C	13: 22,990,024 (GRCm39)	Y222C	possibly damaging	Het
Zfp809	A	G	9: 22,146,347 (GRCm39)	D12G	probably damaging	Het

Other mutations in Dhx30

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01343:Dhx30	APN	9	109,915,313 (GRCm39)	missense	probably benign	0.01
IGL01800:Dhx30	APN	9	109,914,581 (GRCm39)	missense	possibly damaging	0.92
IGL02403:Dhx30	APN	9	109,920,587 (GRCm39)	missense	probably damaging	1.00
IGL02869:Dhx30	APN	9	109,926,251 (GRCm39)	missense	probably damaging	1.00
R0092:Dhx30	UTSW	9	109,914,078 (GRCm39)	missense	possibly damaging	0.94
R0601:Dhx30	UTSW	9	109,915,782 (GRCm39)	splice site	probably null
R1667:Dhx30	UTSW	9	109,914,514 (GRCm39)	missense	possibly damaging	0.48
R1667:Dhx30	UTSW	9	109,914,513 (GRCm39)	missense	possibly damaging	0.91
R1670:Dhx30	UTSW	9	109,914,341 (GRCm39)	missense	possibly damaging	0.86
R1728:Dhx30	UTSW	9	109,927,819 (GRCm39)	missense	probably damaging	0.98
R1729:Dhx30	UTSW	9	109,927,819 (GRCm39)	missense	probably damaging	0.98
R1795:Dhx30	UTSW	9	109,937,051 (GRCm39)	splice site	probably null
R1854:Dhx30	UTSW	9	109,917,740 (GRCm39)	missense	probably damaging	1.00
R2191:Dhx30	UTSW	9	109,915,186 (GRCm39)	critical splice donor site	probably null
R2219:Dhx30	UTSW	9	109,916,703 (GRCm39)	missense	probably damaging	1.00
R2220:Dhx30	UTSW	9	109,916,703 (GRCm39)	missense	probably damaging	1.00
R2267:Dhx30	UTSW	9	109,916,102 (GRCm39)	missense	probably damaging	1.00
R2374:Dhx30	UTSW	9	109,920,632 (GRCm39)	missense	probably damaging	0.98
R2568:Dhx30	UTSW	9	109,926,263 (GRCm39)	missense	probably damaging	0.99
R2881:Dhx30	UTSW	9	109,927,913 (GRCm39)	nonsense	probably null
R4022:Dhx30	UTSW	9	109,913,465 (GRCm39)	missense	possibly damaging	0.90
R4052:Dhx30	UTSW	9	109,929,889 (GRCm39)	missense	possibly damaging	0.46
R4695:Dhx30	UTSW	9	109,914,356 (GRCm39)	missense	probably damaging	0.98
R4728:Dhx30	UTSW	9	109,916,718 (GRCm39)	missense	probably damaging	1.00
R4892:Dhx30	UTSW	9	109,914,924 (GRCm39)	splice site	probably null
R4911:Dhx30	UTSW	9	109,929,992 (GRCm39)	missense	probably damaging	1.00
R4937:Dhx30	UTSW	9	109,915,029 (GRCm39)	missense	probably damaging	1.00
R5135:Dhx30	UTSW	9	109,927,863 (GRCm39)	missense	probably damaging	1.00
R5359:Dhx30	UTSW	9	109,922,203 (GRCm39)	missense	probably damaging	0.99
R5462:Dhx30	UTSW	9	109,930,042 (GRCm39)	missense	probably damaging	0.97
R5504:Dhx30	UTSW	9	109,914,278 (GRCm39)	missense	probably benign	0.08
R5797:Dhx30	UTSW	9	109,927,888 (GRCm39)	missense	probably damaging	0.99
R5860:Dhx30	UTSW	9	109,913,645 (GRCm39)	missense	probably damaging	0.98
R6041:Dhx30	UTSW	9	109,913,666 (GRCm39)	missense	probably benign	0.09
R6132:Dhx30	UTSW	9	109,914,847 (GRCm39)	missense	probably damaging	1.00
R6158:Dhx30	UTSW	9	109,916,098 (GRCm39)	missense	probably damaging	1.00
R6475:Dhx30	UTSW	9	109,914,120 (GRCm39)	missense	possibly damaging	0.91
R6818:Dhx30	UTSW	9	109,917,099 (GRCm39)	missense	probably damaging	1.00
R6984:Dhx30	UTSW	9	109,920,485 (GRCm39)	critical splice donor site	probably null
R7412:Dhx30	UTSW	9	109,921,966 (GRCm39)	missense	probably benign
R7477:Dhx30	UTSW	9	109,916,208 (GRCm39)	missense	probably damaging	1.00
R7808:Dhx30	UTSW	9	109,915,270 (GRCm39)	missense	probably benign	0.00
R7982:Dhx30	UTSW	9	109,914,524 (GRCm39)	missense	probably damaging	1.00
R8343:Dhx30	UTSW	9	109,914,569 (GRCm39)	missense	possibly damaging	0.95
R8376:Dhx30	UTSW	9	109,917,707 (GRCm39)	missense	probably benign	0.15
R8434:Dhx30	UTSW	9	109,929,974 (GRCm39)	missense	probably benign
R8831:Dhx30	UTSW	9	109,917,319 (GRCm39)	missense	probably benign	0.01
R8842:Dhx30	UTSW	9	109,914,296 (GRCm39)	missense	probably benign	0.33
R8971:Dhx30	UTSW	9	109,913,513 (GRCm39)	nonsense	probably null
R9001:Dhx30	UTSW	9	109,916,623 (GRCm39)	missense	probably damaging	0.99
R9117:Dhx30	UTSW	9	109,926,164 (GRCm39)	missense	probably damaging	0.99
R9177:Dhx30	UTSW	9	109,915,750 (GRCm39)	missense	probably damaging	0.97
R9189:Dhx30	UTSW	9	109,914,494 (GRCm39)	nonsense	probably null
R9281:Dhx30	UTSW	9	109,929,983 (GRCm39)	missense	probably benign	0.01
R9289:Dhx30	UTSW	9	109,922,189 (GRCm39)	missense	probably benign	0.06
R9289:Dhx30	UTSW	9	109,920,603 (GRCm39)	missense	possibly damaging	0.66
R9424:Dhx30	UTSW	9	109,916,712 (GRCm39)	missense	probably damaging	1.00
R9576:Dhx30	UTSW	9	109,916,712 (GRCm39)	missense	probably damaging	1.00
R9599:Dhx30	UTSW	9	109,914,518 (GRCm39)	missense	possibly damaging	0.75
R9617:Dhx30	UTSW	9	109,926,186 (GRCm39)	missense	probably damaging	1.00
R9647:Dhx30	UTSW	9	109,922,214 (GRCm39)	missense	probably damaging	1.00
R9711:Dhx30	UTSW	9	109,914,103 (GRCm39)	missense	probably benign	0.03
R9715:Dhx30	UTSW	9	109,916,718 (GRCm39)	missense	probably damaging	1.00
X0027:Dhx30	UTSW	9	109,913,502 (GRCm39)	missense	possibly damaging	0.87
Z1176:Dhx30	UTSW	9	109,916,033 (GRCm39)	missense	probably damaging	0.98

Posted On

2016-08-02