Mutagenetix > Incidental Mutation

Incidental Mutation 'R4802:Vps13c'

472792

Institutional Source

Beutler Lab

Gene Symbol

Vps13c

Ensembl Gene

ENSMUSG00000035284

Gene Name

vacuolar protein sorting 13C

Synonyms

C230055H22Rik

MMRRC Submission

042424-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4802 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

67747678-67902920 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 67871564 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 3244 (F3244L)

Ref Sequence

ENSEMBL: ENSMUSP00000077040 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077879]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000077879
AA Change: F3244L

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

SMART Domains

Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: F3244L

Domain	Start	End	E-Value	Type
Pfam:Chorein_N	3	117	1.3e-39	PFAM
low complexity region	151	165	N/A	INTRINSIC
Pfam:VPS13	182	414	7.9e-70	PFAM
coiled coil region	422	443	N/A	INTRINSIC
low complexity region	479	490	N/A	INTRINSIC
Pfam:VPS13_mid_rpt	611	832	7.8e-71	PFAM
low complexity region	867	885	N/A	INTRINSIC
low complexity region	1020	1036	N/A	INTRINSIC
low complexity region	1112	1123	N/A	INTRINSIC
Pfam:VPS13_mid_rpt	1172	1369	2.1e-14	PFAM
low complexity region	1552	1573	N/A	INTRINSIC
Pfam:VPS13_mid_rpt	1685	1883	2.8e-13	PFAM
Blast:INB	2128	2403	2e-48	BLAST
Pfam:SHR-BD	2759	3013	9.9e-32	PFAM
Pfam:VPS13_C	3317	3495	5.7e-65	PFAM
Pfam:ATG_C	3498	3588	7.9e-12	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000213168
AA Change: F377L

Meta Mutation Damage Score

0.2739

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.3%

Validation Efficiency

97% (93/96)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the vacuolar protein sorting-associated 13 gene family. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]

Allele List at MGI

All alleles(13) : Targeted, other(2) Gene trapped(11)

Other mutations in this stock

Total: 167 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310057J18Rik	A	G	10: 28,859,922 (GRCm39)		probably null	Het
4932416K20Rik	T	A	8: 105,523,664 (GRCm39)		noncoding transcript	Het
Aadacl3	A	G	4: 144,182,802 (GRCm39)	I222T	probably damaging	Het
Abca13	G	T	11: 9,472,341 (GRCm39)	G4249V	possibly damaging	Het
Abcb10	A	G	8: 124,693,266 (GRCm39)	V346A	probably benign	Het
Abcc2	A	T	19: 43,807,800 (GRCm39)	I814F	probably damaging	Het
Alkbh2	C	T	5: 114,262,287 (GRCm39)	E148K	probably damaging	Het
Ankrd28	A	C	14: 31,458,787 (GRCm39)	D335E	probably damaging	Het
Ankrd44	T	C	1: 54,801,475 (GRCm39)	H284R	probably damaging	Het
Arfgef3	G	T	10: 18,467,654 (GRCm39)	Q1849K	probably benign	Het
Bach1	T	A	16: 87,519,340 (GRCm39)	D543E	probably damaging	Het
Bahcc1	G	A	11: 120,173,051 (GRCm39)	V1558I	probably benign	Het
Bbs5	T	A	2: 69,485,958 (GRCm39)	W168R	probably damaging	Het
Bcar3	A	T	3: 122,323,243 (GRCm39)	D766V	probably benign	Het
C1ra	A	G	6: 124,490,727 (GRCm39)	D40G	probably benign	Het
Cbr4	T	C	8: 61,943,113 (GRCm39)		probably benign	Het
Ccdc138	G	A	10: 58,409,465 (GRCm39)	C598Y	probably damaging	Het
Cd200r3	T	A	16: 44,778,188 (GRCm39)	N197K	possibly damaging	Het
Cenpf	T	A	1: 189,383,417 (GRCm39)	E2634D	probably damaging	Het
Cisd2	T	C	3: 135,116,902 (GRCm39)	K63R	probably damaging	Het
Clca3a2	A	T	3: 144,513,112 (GRCm39)	S478T	possibly damaging	Het
Clptm1l	T	C	13: 73,755,981 (GRCm39)	M199T	possibly damaging	Het
Cntnap4	T	A	8: 113,500,222 (GRCm39)	S505T	possibly damaging	Het
Cr2	C	T	1: 194,845,619 (GRCm39)	G112D	probably damaging	Het
Crb2	T	A	2: 37,683,768 (GRCm39)	I1090N	probably benign	Het
Csmd3	G	T	15: 47,484,688 (GRCm39)	P3057Q	probably damaging	Het
Ctso	G	A	3: 81,861,547 (GRCm39)	V307I	probably damaging	Het
Cyp3a41b	T	A	5: 145,510,461 (GRCm39)	T138S	probably benign	Het
Dctn3	G	T	4: 41,719,904 (GRCm39)	Y67*	probably null	Het
Dennd4c	C	A	4: 86,738,121 (GRCm39)	Y918*	probably null	Het
Dlg5	C	T	14: 24,204,757 (GRCm39)	G1262D	probably damaging	Het
Dnaaf1	G	A	8: 120,304,100 (GRCm39)	G46D	probably benign	Het
Dnah6	A	G	6: 73,066,681 (GRCm39)	V2563A	probably damaging	Het
Dnajc13	A	G	9: 104,052,926 (GRCm39)	Y1679H	probably benign	Het
Eif2ak3	T	C	6: 70,864,877 (GRCm39)	Y578H	probably benign	Het
Endod1	C	T	9: 14,268,319 (GRCm39)	V389M	probably benign	Het
Entpd2	T	G	2: 25,289,776 (GRCm39)		probably null	Het
Ephb4	T	C	5: 137,363,768 (GRCm39)	L582P	probably damaging	Het
Eps15	T	C	4: 109,181,414 (GRCm39)	L316S	possibly damaging	Het
Erbb4	G	T	1: 68,369,405 (GRCm39)	T412K	probably damaging	Het
Fam117a	T	A	11: 95,254,896 (GRCm39)	F90I	probably damaging	Het
Fam187b	T	G	7: 30,676,515 (GRCm39)	V8G	possibly damaging	Het
Far1	T	A	7: 113,138,660 (GRCm39)	I59N	possibly damaging	Het
Fbxo34	T	A	14: 47,768,326 (GRCm39)	L562Q	probably damaging	Het
Frem1	T	A	4: 82,834,865 (GRCm39)		probably benign	Het
Gfra3	G	T	18: 34,853,245 (GRCm39)	P10Q	probably damaging	Het
Gm10619	T	A	7: 73,459,773 (GRCm39)		noncoding transcript	Het
Gm19965	T	A	1: 116,749,626 (GRCm39)	Y436N	probably benign	Het
Gm28042	T	C	2: 119,872,535 (GRCm39)		probably benign	Het
Gm4953	A	T	1: 158,995,988 (GRCm39)		noncoding transcript	Het
Gm5799	A	T	14: 43,782,005 (GRCm39)	H59L	probably damaging	Het
Gmppb	T	A	9: 107,927,416 (GRCm39)	V121E	probably benign	Het
Ighv7-4	G	C	12: 114,186,899 (GRCm39)		probably benign	Het
Ipo4	A	G	14: 55,868,671 (GRCm39)	S446P	probably damaging	Het
Itpr2	T	C	6: 146,272,829 (GRCm39)	T855A	probably damaging	Het
Jaml	T	C	9: 45,012,362 (GRCm39)	I283T	possibly damaging	Het
Klhl32	T	C	4: 24,649,698 (GRCm39)	Y399C	possibly damaging	Het
Lratd2	C	A	15: 60,695,793 (GRCm39)		probably benign	Het
Lrriq1	G	A	10: 103,057,179 (GRCm39)	T207I	probably benign	Het
Lrriq3	A	T	3: 154,893,607 (GRCm39)	H436L	probably benign	Het
Mad2l1bp	T	C	17: 46,459,189 (GRCm39)	K114E	possibly damaging	Het
Mamstr	T	C	7: 45,291,842 (GRCm39)	V64A	possibly damaging	Het
Map4	T	A	9: 109,864,325 (GRCm39)	S517T	probably benign	Het
Matn1	A	T	4: 130,677,336 (GRCm39)	I182F	possibly damaging	Het
Mcm3	A	G	1: 20,880,380 (GRCm39)	I484T	probably damaging	Het
Med13	T	A	11: 86,169,599 (GRCm39)	I1922F	probably damaging	Het
Metap2	A	G	10: 93,704,757 (GRCm39)	V137A	probably damaging	Het
Mex3d	A	G	10: 80,222,788 (GRCm39)	V156A	possibly damaging	Het
Mfsd6	G	A	1: 52,748,755 (GRCm39)	P37S	probably benign	Het
Mmut	A	G	17: 41,248,242 (GRCm39)	T90A	probably benign	Het
Mrgprx1	A	C	7: 47,670,959 (GRCm39)	S263A	possibly damaging	Het
Mrtfa	T	C	15: 80,989,000 (GRCm39)	E7G	probably benign	Het
Msantd5f6	C	T	4: 73,319,504 (GRCm39)	W80*	probably null	Het
Msl1	C	T	11: 98,694,795 (GRCm39)	R505*	probably null	Het
Mta2	T	C	19: 8,923,215 (GRCm39)	S96P	probably damaging	Het
Mtr	A	T	13: 12,210,137 (GRCm39)	N986K	probably benign	Het
Mutyh	C	T	4: 116,674,226 (GRCm39)	T259I	probably benign	Het
Myof	T	C	19: 37,934,186 (GRCm39)	T908A	probably benign	Het
Nav2	A	T	7: 49,195,600 (GRCm39)	D992V	possibly damaging	Het
Neb	T	C	2: 52,090,715 (GRCm39)	T1352A	possibly damaging	Het
Nfix	CAAAAA	CAAAA	8: 85,442,876 (GRCm39)		probably null	Het
Nudt19	T	C	7: 35,255,564 (GRCm39)		probably benign	Het
Nudt6	G	A	3: 37,459,503 (GRCm39)	R161C	probably benign	Het
Olr1	A	G	6: 129,465,053 (GRCm39)	F141S	possibly damaging	Het
Oprl1	G	T	2: 181,361,046 (GRCm39)	M340I	probably benign	Het
Or10ag57	T	A	2: 87,218,553 (GRCm39)	V168E	probably benign	Het
Or10d1	T	G	9: 39,484,154 (GRCm39)	M134L	probably benign	Het
Or11g2	A	G	14: 50,856,479 (GRCm39)	T267A	probably benign	Het
Or14j1	T	C	17: 38,146,240 (GRCm39)	Y117H	probably damaging	Het
Or1e17	T	A	11: 73,831,696 (GRCm39)	I208K	possibly damaging	Het
Or2ak6	T	C	11: 58,592,617 (GRCm39)	V30A	probably benign	Het
Or2r2	A	T	6: 42,463,613 (GRCm39)	N171K	probably benign	Het
Or4f53	T	A	2: 111,087,497 (GRCm39)	F12L	probably damaging	Het
Or5d43	T	A	2: 88,105,223 (GRCm39)	M57L	probably damaging	Het
Or5g26	T	A	2: 85,494,622 (GRCm39)	D52V	probably damaging	Het
Or9s15	T	A	1: 92,524,720 (GRCm39)	C160S	probably benign	Het
Otogl	A	C	10: 107,737,197 (GRCm39)	C72W	probably damaging	Het
Pcdha11	T	A	18: 37,138,518 (GRCm39)	I49N	probably damaging	Het
Pcdha4	T	A	18: 37,087,008 (GRCm39)	L397*	probably null	Het
Pcdhb14	A	G	18: 37,581,331 (GRCm39)	S146G	probably benign	Het
Pclo	T	A	5: 14,725,829 (GRCm39)	H1562Q	unknown	Het
Pcsk9	T	C	4: 106,304,766 (GRCm39)	E434G	probably benign	Het
Phc2	A	G	4: 128,645,391 (GRCm39)	K833E	probably damaging	Het
Pja2	A	T	17: 64,599,857 (GRCm39)	S480R	probably damaging	Het
Pkd1	G	A	17: 24,797,070 (GRCm39)	G2493D	probably damaging	Het
Plk5	G	A	10: 80,195,138 (GRCm39)	V179M	possibly damaging	Het
Polr1a	G	A	6: 71,953,054 (GRCm39)	V1541I	probably benign	Het
Ppard	C	G	17: 28,505,348 (GRCm39)	R12G	unknown	Het
Ppp1r14a	A	G	7: 28,990,951 (GRCm39)	D73G	probably damaging	Het
Psd3	C	T	8: 68,573,800 (GRCm39)	R127H	probably benign	Het
Pten	G	T	19: 32,735,903 (GRCm39)	G20V	possibly damaging	Het
Ptprf	G	A	4: 118,067,526 (GRCm39)		probably benign	Het
Rad54l	T	C	4: 115,980,121 (GRCm39)	D21G	probably null	Het
Rgs14	T	C	13: 55,528,770 (GRCm39)	Y304H	probably damaging	Het
Rgs9	T	C	11: 109,131,694 (GRCm39)	K346R	probably damaging	Het
Rnf169	C	G	7: 99,575,653 (GRCm39)	G314A	probably damaging	Het
Rpgrip1l	T	A	8: 91,996,805 (GRCm39)	T692S	probably damaging	Het
Rtf1	T	C	2: 119,505,709 (GRCm39)	V54A	possibly damaging	Het
Rtn4	T	C	11: 29,658,660 (GRCm39)	V938A	probably benign	Het
Ryr2	T	C	13: 11,723,113 (GRCm39)	T2509A	probably damaging	Het
Ryr2	T	A	13: 11,702,818 (GRCm39)	D2890V	probably damaging	Het
Scel	A	C	14: 103,820,536 (GRCm39)	T348P	probably benign	Het
Scgb1b2	G	T	7: 30,990,998 (GRCm39)	L37I	possibly damaging	Het
Sdf4	A	G	4: 156,085,178 (GRCm39)	H171R	possibly damaging	Het
Sec31a	A	G	5: 100,541,222 (GRCm39)	V295A	probably damaging	Het
Semp2l2a	T	A	8: 13,886,970 (GRCm39)	I374F	possibly damaging	Het
Setx	T	A	2: 29,036,385 (GRCm39)	S957T	probably benign	Het
Shroom3	G	T	5: 93,090,945 (GRCm39)	V1151F	probably damaging	Het
Six5	A	G	7: 18,830,894 (GRCm39)	N507S	probably benign	Het
Slc12a7	T	C	13: 73,912,011 (GRCm39)		probably null	Het
Slc1a7	T	A	4: 107,850,237 (GRCm39)	V116E	probably damaging	Het
Slc22a1	A	G	17: 12,894,422 (GRCm39)	L42P	probably damaging	Het
Slc25a31	A	T	3: 40,675,975 (GRCm39)	I174F	probably damaging	Het
Slc31a2	A	T	4: 62,210,869 (GRCm39)	M3L	probably damaging	Het
Slco1a4	T	A	6: 141,791,223 (GRCm39)		probably benign	Het
Smcr8	C	T	11: 60,669,436 (GRCm39)		probably null	Het
Smg5	G	T	3: 88,262,999 (GRCm39)	E801*	probably null	Het
Smgc	C	A	15: 91,738,819 (GRCm39)	H492Q	probably benign	Het
Smyd4	G	T	11: 75,294,010 (GRCm39)	G694V	probably damaging	Het
Sorcs3	A	G	19: 48,387,183 (GRCm39)	T223A	possibly damaging	Het
Stab1	G	T	14: 30,863,328 (GRCm39)	C2119*	probably null	Het
Taar9	A	G	10: 23,984,741 (GRCm39)	I231T	probably damaging	Het
Tacr2	A	G	10: 62,097,327 (GRCm39)	Y269C	probably damaging	Het
Taf3	T	G	2: 9,955,934 (GRCm39)	K744N	possibly damaging	Het
Tarbp1	C	G	8: 127,201,628 (GRCm39)	E59D	possibly damaging	Het
Tcstv1b	T	A	13: 120,634,758 (GRCm39)	S13R	probably benign	Het
Tenm4	T	A	7: 96,555,452 (GRCm39)	V2682E	probably damaging	Het
Tet1	A	C	10: 62,658,442 (GRCm39)	L1468R	probably damaging	Het
Tgfb2	A	T	1: 186,361,110 (GRCm39)	Y380*	probably null	Het
Tgm5	T	G	2: 120,882,953 (GRCm39)	K435Q	probably damaging	Het
Themis	A	G	10: 28,637,507 (GRCm39)	T204A	probably benign	Het
Tm4sf1	T	C	3: 57,202,100 (GRCm39)	Y37C	probably damaging	Het
Tnn	T	C	1: 159,972,603 (GRCm39)	N333S	possibly damaging	Het
Tppp2	A	G	14: 52,156,805 (GRCm39)	N61D	probably benign	Het
Treml2	A	G	17: 48,616,187 (GRCm39)	T276A	probably benign	Het
Trit1	T	C	4: 122,910,431 (GRCm39)	V10A	probably benign	Het
Ttn	T	A	2: 76,794,990 (GRCm39)		probably benign	Het
Uba1y	T	G	Y: 825,890 (GRCm39)		probably null	Het
Vcam1	C	G	3: 115,909,584 (GRCm39)	G581A	probably damaging	Het
Vmn1r16	G	A	6: 57,300,175 (GRCm39)	T149I	probably benign	Het
Vmn1r209	T	C	13: 22,989,826 (GRCm39)	D288G	probably damaging	Het
Vmn1r78	T	A	7: 11,886,891 (GRCm39)	Y167*	probably null	Het
Vmn2r103	T	A	17: 20,015,338 (GRCm39)	S493T	probably benign	Het
Vmn2r105	T	A	17: 20,447,556 (GRCm39)	M423L	probably benign	Het
Zfp119b	A	T	17: 56,246,642 (GRCm39)	D149E	probably damaging	Het
Zfp345	T	C	2: 150,315,228 (GRCm39)	Y103C	possibly damaging	Het
Zmym6	C	T	4: 127,017,009 (GRCm39)	T930I	probably benign	Het

Other mutations in Vps13c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00159:Vps13c	APN	9	67,853,281 (GRCm39)	missense	probably benign	0.20
IGL00336:Vps13c	APN	9	67,853,224 (GRCm39)	missense	probably benign	0.01
IGL00418:Vps13c	APN	9	67,783,544 (GRCm39)	missense	probably damaging	1.00
IGL00481:Vps13c	APN	9	67,768,147 (GRCm39)	missense	probably damaging	1.00
IGL00491:Vps13c	APN	9	67,800,418 (GRCm39)	missense	probably damaging	1.00
IGL00558:Vps13c	APN	9	67,845,139 (GRCm39)	missense	possibly damaging	0.52
IGL00811:Vps13c	APN	9	67,855,463 (GRCm39)	missense	probably damaging	0.99
IGL01011:Vps13c	APN	9	67,834,237 (GRCm39)	missense	probably damaging	0.98
IGL01094:Vps13c	APN	9	67,793,566 (GRCm39)	missense	probably damaging	1.00
IGL01330:Vps13c	APN	9	67,871,390 (GRCm39)	missense	probably damaging	1.00
IGL01402:Vps13c	APN	9	67,820,486 (GRCm39)	critical splice acceptor site	probably null
IGL01404:Vps13c	APN	9	67,820,486 (GRCm39)	critical splice acceptor site	probably null
IGL01470:Vps13c	APN	9	67,820,209 (GRCm39)	splice site	probably benign
IGL01615:Vps13c	APN	9	67,863,063 (GRCm39)	missense	probably benign	0.01
IGL01694:Vps13c	APN	9	67,802,631 (GRCm39)	missense	probably damaging	1.00
IGL01752:Vps13c	APN	9	67,855,510 (GRCm39)	missense	probably damaging	1.00
IGL01810:Vps13c	APN	9	67,863,062 (GRCm39)	missense	probably benign
IGL01954:Vps13c	APN	9	67,876,580 (GRCm39)	missense	probably damaging	0.98
IGL01978:Vps13c	APN	9	67,837,925 (GRCm39)	missense	probably benign	0.03
IGL01998:Vps13c	APN	9	67,862,350 (GRCm39)	splice site	probably null
IGL02201:Vps13c	APN	9	67,874,418 (GRCm39)	missense	probably damaging	1.00
IGL02205:Vps13c	APN	9	67,790,736 (GRCm39)	missense	probably damaging	1.00
IGL02303:Vps13c	APN	9	67,852,763 (GRCm39)	splice site	probably benign
IGL02322:Vps13c	APN	9	67,845,183 (GRCm39)	missense	probably benign	0.02
IGL02456:Vps13c	APN	9	67,860,258 (GRCm39)	missense	probably damaging	1.00
IGL02474:Vps13c	APN	9	67,845,158 (GRCm39)	missense	probably benign	0.00
IGL02547:Vps13c	APN	9	67,815,301 (GRCm39)	missense	possibly damaging	0.83
IGL02640:Vps13c	APN	9	67,793,530 (GRCm39)	splice site	probably benign
IGL02673:Vps13c	APN	9	67,785,380 (GRCm39)	missense	probably damaging	1.00
IGL02721:Vps13c	APN	9	67,871,431 (GRCm39)	splice site	probably benign
IGL02834:Vps13c	APN	9	67,845,137 (GRCm39)	missense	probably benign
IGL02838:Vps13c	APN	9	67,883,133 (GRCm39)	missense	probably damaging	1.00
IGL03136:Vps13c	APN	9	67,857,592 (GRCm39)	missense	probably damaging	1.00
IGL03137:Vps13c	APN	9	67,797,662 (GRCm39)	missense	probably damaging	1.00
IGL03214:Vps13c	APN	9	67,804,477 (GRCm39)	missense	probably null	0.81
IGL03240:Vps13c	APN	9	67,862,329 (GRCm39)	missense	probably benign
IGL03303:Vps13c	APN	9	67,841,786 (GRCm39)	missense	probably benign	0.27
IGL03336:Vps13c	APN	9	67,858,924 (GRCm39)	missense	possibly damaging	0.76
IGL03366:Vps13c	APN	9	67,853,308 (GRCm39)	missense	probably benign	0.00
Derivative	UTSW	9	67,837,904 (GRCm39)	missense	possibly damaging	0.79
diversion	UTSW	9	67,817,515 (GRCm39)	missense	possibly damaging	0.93
introversion	UTSW	9	67,851,328 (GRCm39)	missense	probably damaging	0.98
Inversion	UTSW	9	67,810,121 (GRCm39)	critical splice acceptor site	probably null
subversion	UTSW	9	67,815,334 (GRCm39)	missense	probably damaging	1.00
Transversion	UTSW	9	67,841,783 (GRCm39)	missense	probably damaging	0.98
3-1:Vps13c	UTSW	9	67,843,655 (GRCm39)	missense	probably benign	0.00
IGL02991:Vps13c	UTSW	9	67,821,159 (GRCm39)	missense	probably damaging	1.00
PIT4802001:Vps13c	UTSW	9	67,845,068 (GRCm39)	missense	probably damaging	1.00
R0008:Vps13c	UTSW	9	67,826,544 (GRCm39)	missense	probably benign
R0206:Vps13c	UTSW	9	67,846,444 (GRCm39)	splice site	probably benign
R0288:Vps13c	UTSW	9	67,834,648 (GRCm39)	missense	probably damaging	0.99
R0324:Vps13c	UTSW	9	67,871,591 (GRCm39)	missense	possibly damaging	0.95
R0347:Vps13c	UTSW	9	67,817,515 (GRCm39)	missense	possibly damaging	0.93
R0374:Vps13c	UTSW	9	67,793,528 (GRCm39)	splice site	probably benign
R0388:Vps13c	UTSW	9	67,830,197 (GRCm39)	splice site	probably benign
R0409:Vps13c	UTSW	9	67,858,926 (GRCm39)	missense	probably benign	0.00
R0440:Vps13c	UTSW	9	67,880,143 (GRCm39)	missense	probably damaging	1.00
R0513:Vps13c	UTSW	9	67,838,017 (GRCm39)	missense	probably benign	0.02
R0520:Vps13c	UTSW	9	67,853,133 (GRCm39)	missense	possibly damaging	0.88
R0569:Vps13c	UTSW	9	67,881,001 (GRCm39)	missense	probably damaging	0.98
R0601:Vps13c	UTSW	9	67,834,754 (GRCm39)	missense	probably benign	0.12
R0659:Vps13c	UTSW	9	67,828,217 (GRCm39)	missense	probably benign	0.11
R0667:Vps13c	UTSW	9	67,858,855 (GRCm39)	nonsense	probably null
R0670:Vps13c	UTSW	9	67,833,139 (GRCm39)	missense	probably benign	0.35
R0698:Vps13c	UTSW	9	67,797,005 (GRCm39)	missense	probably benign	0.45
R0729:Vps13c	UTSW	9	67,868,931 (GRCm39)	missense	probably damaging	1.00
R0781:Vps13c	UTSW	9	67,879,285 (GRCm39)	missense	probably damaging	1.00
R0811:Vps13c	UTSW	9	67,841,758 (GRCm39)	missense	probably benign	0.06
R0812:Vps13c	UTSW	9	67,841,758 (GRCm39)	missense	probably benign	0.06
R0839:Vps13c	UTSW	9	67,806,020 (GRCm39)	missense	probably benign
R1373:Vps13c	UTSW	9	67,834,793 (GRCm39)	missense	probably damaging	0.99
R1396:Vps13c	UTSW	9	67,862,304 (GRCm39)	missense	probably benign	0.00
R1499:Vps13c	UTSW	9	67,864,787 (GRCm39)	missense	probably benign	0.00
R1556:Vps13c	UTSW	9	67,837,993 (GRCm39)	missense	probably damaging	0.98
R1560:Vps13c	UTSW	9	67,843,745 (GRCm39)	critical splice donor site	probably null
R1584:Vps13c	UTSW	9	67,800,394 (GRCm39)	missense	possibly damaging	0.74
R1654:Vps13c	UTSW	9	67,858,969 (GRCm39)	missense	probably damaging	1.00
R1674:Vps13c	UTSW	9	67,760,985 (GRCm39)	nonsense	probably null
R1676:Vps13c	UTSW	9	67,834,244 (GRCm39)	missense	probably benign	0.20
R1695:Vps13c	UTSW	9	67,879,357 (GRCm39)	nonsense	probably null
R1710:Vps13c	UTSW	9	67,818,811 (GRCm39)	missense	probably benign	0.00
R1769:Vps13c	UTSW	9	67,873,003 (GRCm39)	missense	probably benign	0.00
R1775:Vps13c	UTSW	9	67,788,729 (GRCm39)	missense	probably damaging	1.00
R1795:Vps13c	UTSW	9	67,801,267 (GRCm39)	nonsense	probably null
R1799:Vps13c	UTSW	9	67,851,399 (GRCm39)	missense	probably damaging	0.98
R1835:Vps13c	UTSW	9	67,900,295 (GRCm39)	missense	probably benign	0.08
R1848:Vps13c	UTSW	9	67,843,622 (GRCm39)	missense	probably benign
R1903:Vps13c	UTSW	9	67,801,334 (GRCm39)	missense	probably damaging	1.00
R1944:Vps13c	UTSW	9	67,793,558 (GRCm39)	missense	probably damaging	1.00
R1945:Vps13c	UTSW	9	67,793,558 (GRCm39)	missense	probably damaging	1.00
R1951:Vps13c	UTSW	9	67,881,041 (GRCm39)	critical splice donor site	probably null
R1993:Vps13c	UTSW	9	67,883,138 (GRCm39)	missense	probably damaging	1.00
R2023:Vps13c	UTSW	9	67,843,567 (GRCm39)	splice site	probably benign
R2059:Vps13c	UTSW	9	67,768,115 (GRCm39)	missense	probably damaging	1.00
R2086:Vps13c	UTSW	9	67,857,571 (GRCm39)	missense	probably benign	0.29
R2120:Vps13c	UTSW	9	67,826,616 (GRCm39)	missense	possibly damaging	0.92
R2249:Vps13c	UTSW	9	67,895,335 (GRCm39)	critical splice donor site	probably null
R2257:Vps13c	UTSW	9	67,860,228 (GRCm39)	missense	possibly damaging	0.87
R2258:Vps13c	UTSW	9	67,861,142 (GRCm39)	missense	probably benign	0.01
R2259:Vps13c	UTSW	9	67,861,142 (GRCm39)	missense	probably benign	0.01
R2260:Vps13c	UTSW	9	67,861,142 (GRCm39)	missense	probably benign	0.01
R2265:Vps13c	UTSW	9	67,828,229 (GRCm39)	missense	possibly damaging	0.82
R2266:Vps13c	UTSW	9	67,828,229 (GRCm39)	missense	possibly damaging	0.82
R2269:Vps13c	UTSW	9	67,828,229 (GRCm39)	missense	possibly damaging	0.82
R2278:Vps13c	UTSW	9	67,846,354 (GRCm39)	missense	probably benign
R2306:Vps13c	UTSW	9	67,895,275 (GRCm39)	missense	probably damaging	0.99
R2327:Vps13c	UTSW	9	67,821,102 (GRCm39)	missense	probably damaging	0.98
R2349:Vps13c	UTSW	9	67,864,808 (GRCm39)	missense	possibly damaging	0.89
R2483:Vps13c	UTSW	9	67,883,189 (GRCm39)	critical splice donor site	probably null
R3031:Vps13c	UTSW	9	67,831,052 (GRCm39)	missense	probably benign	0.00
R3623:Vps13c	UTSW	9	67,883,189 (GRCm39)	critical splice donor site	probably null
R3870:Vps13c	UTSW	9	67,792,008 (GRCm39)	missense	probably benign	0.00
R4173:Vps13c	UTSW	9	67,843,595 (GRCm39)	missense	probably benign	0.00
R4445:Vps13c	UTSW	9	67,889,777 (GRCm39)	splice site	probably null
R4491:Vps13c	UTSW	9	67,817,475 (GRCm39)	missense	probably benign
R4505:Vps13c	UTSW	9	67,846,316 (GRCm39)	missense	probably benign	0.02
R4574:Vps13c	UTSW	9	67,858,965 (GRCm39)	missense	probably damaging	1.00
R4691:Vps13c	UTSW	9	67,860,217 (GRCm39)	missense	possibly damaging	0.95
R4766:Vps13c	UTSW	9	67,785,506 (GRCm39)	splice site	probably null
R4771:Vps13c	UTSW	9	67,836,821 (GRCm39)	missense	probably benign
R4801:Vps13c	UTSW	9	67,871,564 (GRCm39)	missense	probably damaging	1.00
R4962:Vps13c	UTSW	9	67,781,173 (GRCm39)	missense	probably damaging	1.00
R4995:Vps13c	UTSW	9	67,826,603 (GRCm39)	missense	probably benign	0.00
R5010:Vps13c	UTSW	9	67,823,661 (GRCm39)	missense	probably benign	0.19
R5183:Vps13c	UTSW	9	67,815,334 (GRCm39)	missense	probably damaging	1.00
R5226:Vps13c	UTSW	9	67,852,835 (GRCm39)	missense	probably benign	0.17
R5297:Vps13c	UTSW	9	67,785,413 (GRCm39)	missense	probably damaging	1.00
R5456:Vps13c	UTSW	9	67,834,729 (GRCm39)	missense	possibly damaging	0.53
R5494:Vps13c	UTSW	9	67,855,428 (GRCm39)	missense	probably benign	0.00
R5521:Vps13c	UTSW	9	67,858,721 (GRCm39)	missense	probably benign	0.08
R5524:Vps13c	UTSW	9	67,864,838 (GRCm39)	missense	probably damaging	1.00
R5685:Vps13c	UTSW	9	67,870,455 (GRCm39)	missense	possibly damaging	0.64
R5731:Vps13c	UTSW	9	67,802,661 (GRCm39)	missense	probably damaging	1.00
R5812:Vps13c	UTSW	9	67,889,777 (GRCm39)	splice site	probably benign
R5867:Vps13c	UTSW	9	67,889,904 (GRCm39)	splice site	probably null
R5893:Vps13c	UTSW	9	67,810,121 (GRCm39)	critical splice acceptor site	probably null
R5902:Vps13c	UTSW	9	67,841,729 (GRCm39)	missense	probably benign	0.00
R5957:Vps13c	UTSW	9	67,862,253 (GRCm39)	missense	probably damaging	1.00
R6076:Vps13c	UTSW	9	67,818,884 (GRCm39)	missense	probably damaging	1.00
R6187:Vps13c	UTSW	9	67,822,939 (GRCm39)	missense	probably damaging	1.00
R6268:Vps13c	UTSW	9	67,858,731 (GRCm39)	missense	probably benign	0.10
R6547:Vps13c	UTSW	9	67,880,647 (GRCm39)	missense	probably damaging	1.00
R6716:Vps13c	UTSW	9	67,858,749 (GRCm39)	missense	probably benign	0.00
R6837:Vps13c	UTSW	9	67,817,504 (GRCm39)	missense	probably benign
R6919:Vps13c	UTSW	9	67,834,734 (GRCm39)	missense	probably damaging	0.97
R7039:Vps13c	UTSW	9	67,845,045 (GRCm39)	missense	probably damaging	1.00
R7058:Vps13c	UTSW	9	67,831,110 (GRCm39)	missense	probably benign	0.39
R7082:Vps13c	UTSW	9	67,790,735 (GRCm39)	missense	probably damaging	1.00
R7195:Vps13c	UTSW	9	67,853,107 (GRCm39)	missense	possibly damaging	0.95
R7244:Vps13c	UTSW	9	67,797,086 (GRCm39)	missense	probably benign	0.00
R7300:Vps13c	UTSW	9	67,847,826 (GRCm39)	missense	probably benign	0.20
R7314:Vps13c	UTSW	9	67,850,622 (GRCm39)	splice site	probably null
R7352:Vps13c	UTSW	9	67,747,728 (GRCm39)	missense	possibly damaging	0.94
R7368:Vps13c	UTSW	9	67,821,355 (GRCm39)	missense	probably benign	0.23
R7411:Vps13c	UTSW	9	67,879,283 (GRCm39)	missense	probably damaging	0.98
R7497:Vps13c	UTSW	9	67,747,761 (GRCm39)	missense	probably damaging	1.00
R7516:Vps13c	UTSW	9	67,862,289 (GRCm39)	missense	possibly damaging	0.89
R7638:Vps13c	UTSW	9	67,852,791 (GRCm39)	missense	probably damaging	1.00
R7732:Vps13c	UTSW	9	67,847,798 (GRCm39)	missense	probably damaging	0.97
R7748:Vps13c	UTSW	9	67,870,371 (GRCm39)	missense	probably benign	0.03
R7779:Vps13c	UTSW	9	67,788,704 (GRCm39)	missense	probably damaging	1.00
R7788:Vps13c	UTSW	9	67,847,765 (GRCm39)	missense	probably benign	0.01
R7894:Vps13c	UTSW	9	67,834,265 (GRCm39)	missense	probably damaging	0.99
R8163:Vps13c	UTSW	9	67,857,720 (GRCm39)	missense	probably benign	0.08
R8165:Vps13c	UTSW	9	67,766,072 (GRCm39)	missense	probably benign	0.00
R8202:Vps13c	UTSW	9	67,851,328 (GRCm39)	missense	probably damaging	0.98
R8235:Vps13c	UTSW	9	67,863,063 (GRCm39)	missense	probably benign	0.01
R8235:Vps13c	UTSW	9	67,834,678 (GRCm39)	missense	probably damaging	1.00
R8253:Vps13c	UTSW	9	67,850,770 (GRCm39)	nonsense	probably null
R8261:Vps13c	UTSW	9	67,862,262 (GRCm39)	missense	probably damaging	1.00
R8348:Vps13c	UTSW	9	67,786,385 (GRCm39)	missense	possibly damaging	0.79
R8547:Vps13c	UTSW	9	67,852,848 (GRCm39)	missense	probably damaging	1.00
R8734:Vps13c	UTSW	9	67,880,685 (GRCm39)	missense	probably damaging	1.00
R8806:Vps13c	UTSW	9	67,853,110 (GRCm39)	missense	probably damaging	1.00
R8807:Vps13c	UTSW	9	67,766,122 (GRCm39)	missense	probably damaging	0.99
R8813:Vps13c	UTSW	9	67,778,566 (GRCm39)	missense	probably damaging	1.00
R8883:Vps13c	UTSW	9	67,855,479 (GRCm39)	missense	probably benign	0.10
R8885:Vps13c	UTSW	9	67,850,736 (GRCm39)	missense	probably benign
R8899:Vps13c	UTSW	9	67,841,783 (GRCm39)	missense	probably damaging	0.98
R8970:Vps13c	UTSW	9	67,852,803 (GRCm39)	missense	probably benign	0.11
R9007:Vps13c	UTSW	9	67,845,006 (GRCm39)	missense	probably benign	0.00
R9026:Vps13c	UTSW	9	67,861,863 (GRCm39)	missense	probably damaging	1.00
R9029:Vps13c	UTSW	9	67,855,429 (GRCm39)	missense	probably damaging	0.98
R9057:Vps13c	UTSW	9	67,828,209 (GRCm39)	missense	probably benign	0.00
R9105:Vps13c	UTSW	9	67,778,081 (GRCm39)	intron	probably benign
R9130:Vps13c	UTSW	9	67,836,805 (GRCm39)	missense	probably damaging	1.00
R9286:Vps13c	UTSW	9	67,880,203 (GRCm39)	missense	probably benign	0.00
R9338:Vps13c	UTSW	9	67,858,977 (GRCm39)	missense	probably damaging	1.00
R9432:Vps13c	UTSW	9	67,830,137 (GRCm39)	missense	probably benign	0.02
R9460:Vps13c	UTSW	9	67,837,904 (GRCm39)	missense	possibly damaging	0.79
R9464:Vps13c	UTSW	9	67,858,674 (GRCm39)	missense	probably damaging	1.00
R9561:Vps13c	UTSW	9	67,872,794 (GRCm39)	missense	probably damaging	1.00
R9609:Vps13c	UTSW	9	67,841,831 (GRCm39)	missense	probably damaging	1.00
R9622:Vps13c	UTSW	9	67,856,715 (GRCm39)	missense	probably damaging	1.00
R9665:Vps13c	UTSW	9	67,863,025 (GRCm39)	nonsense	probably null
R9731:Vps13c	UTSW	9	67,826,526 (GRCm39)	missense	probably benign
R9763:Vps13c	UTSW	9	67,818,860 (GRCm39)	missense	probably benign	0.00
R9774:Vps13c	UTSW	9	67,791,873 (GRCm39)	missense	possibly damaging	0.85
R9798:Vps13c	UTSW	9	67,826,646 (GRCm39)	missense	probably damaging	1.00
U24488:Vps13c	UTSW	9	67,813,198 (GRCm39)	missense	probably benign	0.13
X0021:Vps13c	UTSW	9	67,845,063 (GRCm39)	missense	probably damaging	0.99
X0058:Vps13c	UTSW	9	67,834,701 (GRCm39)	missense	probably damaging	1.00
X0065:Vps13c	UTSW	9	67,781,145 (GRCm39)	missense	probably damaging	1.00
Z1088:Vps13c	UTSW	9	67,821,257 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2017-04-14