Mutagenetix > Incidental Mutation

Incidental Mutation 'R7244:Vps13c'

563420

Institutional Source

Beutler Lab

Gene Symbol

Vps13c

Ensembl Gene

ENSMUSG00000035284

Gene Name

vacuolar protein sorting 13C

Synonyms

C230055H22Rik

MMRRC Submission

045308-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7244 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

67747678-67902920 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 67797086 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 491 (V491A)

Ref Sequence

ENSEMBL: ENSMUSP00000077040 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077879] [ENSMUST00000217386]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000077879
AA Change: V491A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: V491A

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

probably benign
Transcript: ENSMUST00000217386
AA Change: V491A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

96% (45/47)

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: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrb3	A	G	1: 25,170,350 (GRCm39)	F983L	probably damaging	Het
Cc2d1b	T	A	4: 108,486,799 (GRCm39)	M632K	probably benign	Het
Cdyl2	G	A	8: 117,301,999 (GRCm39)	R461*	probably null	Het
Cfap57	G	A	4: 118,411,997 (GRCm39)	Q1216*	probably null	Het
Chd1l	A	T	3: 97,505,066 (GRCm39)	V167E	probably damaging	Het
Col6a1	C	A	10: 76,553,242 (GRCm39)	G391*	probably null	Het
Ctsc	C	A	7: 87,951,430 (GRCm39)	Q226K	probably benign	Het
Cyp2c54	A	G	19: 40,035,953 (GRCm39)	V319A	probably damaging	Het
Dnah7b	T	C	1: 46,316,303 (GRCm39)	S3139P	probably damaging	Het
Edrf1	T	C	7: 133,256,079 (GRCm39)	S643P	probably benign	Het
Fam186a	A	T	15: 99,844,273 (GRCm39)	V657D	unknown	Het
Fkbp11	A	G	15: 98,626,073 (GRCm39)		probably benign	Het
Fsip2	G	A	2: 82,823,607 (GRCm39)	A6447T	possibly damaging	Het
H2-T9	C	A	17: 36,438,496 (GRCm39)		probably null	Het
Hydin	A	G	8: 111,276,307 (GRCm39)	D3017G	probably damaging	Het
Ifi205	G	A	1: 173,845,210 (GRCm39)	Q191*	probably null	Het
Mbd4	C	T	6: 115,821,564 (GRCm39)	D484N	probably benign	Het
Med24	C	T	11: 98,605,223 (GRCm39)		probably null	Het
Mis18bp1	T	C	12: 65,208,404 (GRCm39)	N103S	probably damaging	Het
Mmd2	T	C	5: 142,550,587 (GRCm39)	H217R	probably damaging	Het
Mn1	C	T	5: 111,566,699 (GRCm39)	T223M	possibly damaging	Het
Ms4a4a	A	G	19: 11,358,794 (GRCm39)	Y84C	probably damaging	Het
Mup5	A	T	4: 61,749,818 (GRCm39)		probably null	Het
Mybl2	C	T	2: 162,924,605 (GRCm39)	P658S	probably benign	Het
Mycbp2	C	A	14: 103,446,345 (GRCm39)	V1828L	probably damaging	Het
Myh15	T	C	16: 49,017,149 (GRCm39)	Y1887H	probably damaging	Het
Nadk2	A	G	15: 9,083,271 (GRCm39)		probably null	Het
Nsd3	A	G	8: 26,156,055 (GRCm39)	N541D	probably damaging	Het
Or52e8b	A	G	7: 104,674,148 (GRCm39)	V13A	probably benign	Het
Or52i2	G	T	7: 102,319,046 (GRCm39)		probably benign	Het
Oxa1l	A	T	14: 54,598,312 (GRCm39)	M1L	probably benign	Het
Pcdha11	A	T	18: 37,144,421 (GRCm39)	R171*	probably null	Het
Pkd1l1	A	T	11: 8,821,771 (GRCm39)	V1641E		Het
Pramel28	A	T	4: 143,692,455 (GRCm39)	M182K	probably benign	Het
Prom1	T	A	5: 44,178,242 (GRCm39)	I497L	probably benign	Het
Rasgef1b	T	C	5: 99,706,753 (GRCm39)	K41E	possibly damaging	Het
Rasgrf1	T	C	9: 89,876,810 (GRCm39)	F725S	probably damaging	Het
Ryr2	T	A	13: 11,612,032 (GRCm39)	S3962C	probably damaging	Het
Sema5b	A	T	16: 35,480,915 (GRCm39)	T829S	probably benign	Het
Tdp2	A	G	13: 25,025,284 (GRCm39)	D351G	probably benign	Het
Tet3	A	T	6: 83,347,603 (GRCm39)	D1130E	probably damaging	Het
Tg	T	C	15: 66,612,563 (GRCm39)	C1993R	probably damaging	Het
Tll1	T	C	8: 64,478,222 (GRCm39)	I844V	probably benign	Het
Ttll13	A	C	7: 79,903,911 (GRCm39)	K280Q	probably damaging	Het
Vmn2r109	A	G	17: 20,760,945 (GRCm39)	V804A	possibly damaging	Het
Xpo5	G	T	17: 46,525,551 (GRCm39)	G233C	probably damaging	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
R4802: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
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

PCR Primer
(F):5'- CCATACATAGACTTAACGGTGAAC -3'
(R):5'- ATAAGGAGCACTGGACGCTG -3'

Sequencing Primer
(F):5'- GACTTAACGGTGAACAGTGTTTC -3'
(R):5'- TGGACGCTGAGACCCCTAAG -3'

Posted On

2019-06-26