Mutagenetix > Incidental Mutation

Incidental Mutation 'R1396:Vps13c'

162651

Institutional Source

Beutler Lab

Gene Symbol

Vps13c

Ensembl Gene

ENSMUSG00000035284

Gene Name

vacuolar protein sorting 13C

Synonyms

C230055H22Rik

MMRRC Submission

039458-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1396 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

67840396-67995638 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 67955022 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 2974 (I2974V)

Ref Sequence

ENSEMBL: ENSMUSP00000077040 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000077879
AA Change: I2974V

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: I2974V

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: I107V

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.3%
20x: 89.4%

Validation Efficiency

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: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921530L21Rik	A	G	14: 95,882,551 (GRCm38)	N248S	probably benign	Het
4930486L24Rik	G	A	13: 60,853,243 (GRCm38)	P160S	probably benign	Het
Adamts12	G	T	15: 11,311,472 (GRCm38)	D1272Y	probably benign	Het
Akr1c20	A	T	13: 4,507,727 (GRCm38)	V267D	probably damaging	Het
C1s1	A	G	6: 124,531,051 (GRCm38)	S660P	probably damaging	Het
Ccdc40	A	G	11: 119,231,803 (GRCm38)	T144A	possibly damaging	Het
Cdk20	T	C	13: 64,437,403 (GRCm38)	I167T	probably damaging	Het
Chd6	A	G	2: 160,983,103 (GRCm38)	L1212S	probably damaging	Het
Clock	G	C	5: 76,266,802 (GRCm38)	D15E	probably benign	Het
Clstn2	A	G	9: 97,461,393 (GRCm38)	V667A	probably benign	Het
Cr2	A	T	1: 195,169,253 (GRCm38)		probably null	Het
Cyp2e1	A	G	7: 140,773,079 (GRCm38)	D343G	probably damaging	Het
Dync1h1	G	A	12: 110,636,509 (GRCm38)	E2195K	probably benign	Het
Etf1	G	A	18: 34,908,167 (GRCm38)	T298I	possibly damaging	Het
Gm5431	T	C	11: 48,895,434 (GRCm38)		probably benign	Het
Gss	G	A	2: 155,567,721 (GRCm38)	T265I	probably damaging	Het
Heatr1	C	T	13: 12,406,046 (GRCm38)	S406L	possibly damaging	Het
Hgsnat	C	A	8: 25,957,335 (GRCm38)	M310I	possibly damaging	Het
Inpp5b	G	A	4: 124,789,080 (GRCm38)	R598H	probably damaging	Het
Ints2	G	T	11: 86,249,248 (GRCm38)	Q253K	probably damaging	Het
Kng1	A	G	16: 23,078,980 (GRCm38)	M377V	probably benign	Het
Krt72	C	T	15: 101,786,005 (GRCm38)		probably null	Het
Lemd2	G	C	17: 27,190,732 (GRCm38)	R482G	probably damaging	Het
Lrpprc	C	T	17: 84,726,303 (GRCm38)	D1049N	possibly damaging	Het
Lrrc49	A	T	9: 60,680,527 (GRCm38)	H117Q	probably damaging	Het
Mcm6	A	T	1: 128,351,476 (GRCm38)	F191Y	probably damaging	Het
Mecom	T	C	3: 29,979,800 (GRCm38)	T252A	possibly damaging	Het
Mgat4e	T	C	1: 134,541,533 (GRCm38)	T258A	probably benign	Het
Mpeg1	A	G	19: 12,462,804 (GRCm38)	N542S	probably damaging	Het
Nln	C	T	13: 104,061,753 (GRCm38)	V184I	probably benign	Het
Nova1	A	C	12: 46,816,893 (GRCm38)	F91L	unknown	Het
Polk	T	C	13: 96,484,208 (GRCm38)	I516V	probably benign	Het
Ppig	C	T	2: 69,749,018 (GRCm38)	P357S	unknown	Het
Ptpro	T	A	6: 137,443,594 (GRCm38)	V1007D	probably damaging	Het
Rasal2	A	T	1: 157,164,666 (GRCm38)	H552Q	probably damaging	Het
Rnf41	G	A	10: 128,435,571 (GRCm38)	E117K	probably benign	Het
Sbk3	A	G	7: 4,967,453 (GRCm38)	Y306H	possibly damaging	Het
Senp1	A	G	15: 98,076,554 (GRCm38)	S126P	probably benign	Het
Sfr1	A	G	19: 47,733,690 (GRCm38)	K182E	probably benign	Het
Slc25a4	C	A	8: 46,209,288 (GRCm38)	R111L	probably damaging	Het
Slc9c1	A	T	16: 45,573,347 (GRCm38)	Y551F	probably benign	Het
Stard4	A	T	18: 33,206,210 (GRCm38)	N80K	probably damaging	Het
Tbk1	G	A	10: 121,571,916 (GRCm38)	T104M	probably damaging	Het
Tedc2	T	A	17: 24,216,317 (GRCm38)	E366V	probably damaging	Het
Tedc2	C	A	17: 24,216,318 (GRCm38)	E366*	probably null	Het
Tmem102	A	T	11: 69,804,370 (GRCm38)	W259R	probably damaging	Het
Tnk1	A	T	11: 69,853,136 (GRCm38)	C466S	probably benign	Het
Tspoap1	A	C	11: 87,766,120 (GRCm38)	Q307P	probably damaging	Het
Ugt2b35	A	G	5: 87,011,530 (GRCm38)	N528D	possibly damaging	Het
Usp6nl	A	G	2: 6,426,998 (GRCm38)		probably null	Het
Vmn1r203	C	T	13: 22,524,508 (GRCm38)	T153M	probably benign	Het
Vmn1r89	T	A	7: 13,220,011 (GRCm38)	S157T	probably damaging	Het
Vmn2r103	A	T	17: 19,792,968 (GRCm38)	Y117F	probably benign	Het
Vmn2r116	A	C	17: 23,386,141 (GRCm38)	M143L	probably benign	Het
Vmn2r62	A	T	7: 42,764,837 (GRCm38)	D727E	probably damaging	Het
Wrn	C	T	8: 33,268,819 (GRCm38)	G769D	probably damaging	Het
Zhx3	T	A	2: 160,781,020 (GRCm38)	H409L	possibly damaging	Het

Other mutations in Vps13c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00159:Vps13c	APN	9	67,945,999 (GRCm38)	missense	probably benign	0.20
IGL00336:Vps13c	APN	9	67,945,942 (GRCm38)	missense	probably benign	0.01
IGL00418:Vps13c	APN	9	67,876,262 (GRCm38)	missense	probably damaging	1.00
IGL00481:Vps13c	APN	9	67,860,865 (GRCm38)	missense	probably damaging	1.00
IGL00491:Vps13c	APN	9	67,893,136 (GRCm38)	missense	probably damaging	1.00
IGL00558:Vps13c	APN	9	67,937,857 (GRCm38)	missense	possibly damaging	0.52
IGL00811:Vps13c	APN	9	67,948,181 (GRCm38)	missense	probably damaging	0.99
IGL01011:Vps13c	APN	9	67,926,955 (GRCm38)	missense	probably damaging	0.98
IGL01094:Vps13c	APN	9	67,886,284 (GRCm38)	missense	probably damaging	1.00
IGL01330:Vps13c	APN	9	67,964,108 (GRCm38)	missense	probably damaging	1.00
IGL01402:Vps13c	APN	9	67,913,204 (GRCm38)	critical splice acceptor site	probably null
IGL01404:Vps13c	APN	9	67,913,204 (GRCm38)	critical splice acceptor site	probably null
IGL01470:Vps13c	APN	9	67,912,927 (GRCm38)	splice site	probably benign
IGL01615:Vps13c	APN	9	67,955,781 (GRCm38)	missense	probably benign	0.01
IGL01694:Vps13c	APN	9	67,895,349 (GRCm38)	missense	probably damaging	1.00
IGL01752:Vps13c	APN	9	67,948,228 (GRCm38)	missense	probably damaging	1.00
IGL01810:Vps13c	APN	9	67,955,780 (GRCm38)	missense	probably benign
IGL01954:Vps13c	APN	9	67,969,298 (GRCm38)	missense	probably damaging	0.98
IGL01978:Vps13c	APN	9	67,930,643 (GRCm38)	missense	probably benign	0.03
IGL01998:Vps13c	APN	9	67,955,068 (GRCm38)	splice site	probably null
IGL02201:Vps13c	APN	9	67,967,136 (GRCm38)	missense	probably damaging	1.00
IGL02205:Vps13c	APN	9	67,883,454 (GRCm38)	missense	probably damaging	1.00
IGL02303:Vps13c	APN	9	67,945,481 (GRCm38)	splice site	probably benign
IGL02322:Vps13c	APN	9	67,937,901 (GRCm38)	missense	probably benign	0.02
IGL02456:Vps13c	APN	9	67,952,976 (GRCm38)	missense	probably damaging	1.00
IGL02474:Vps13c	APN	9	67,937,876 (GRCm38)	missense	probably benign	0.00
IGL02547:Vps13c	APN	9	67,908,019 (GRCm38)	missense	possibly damaging	0.83
IGL02640:Vps13c	APN	9	67,886,248 (GRCm38)	splice site	probably benign
IGL02673:Vps13c	APN	9	67,878,098 (GRCm38)	missense	probably damaging	1.00
IGL02721:Vps13c	APN	9	67,964,149 (GRCm38)	splice site	probably benign
IGL02834:Vps13c	APN	9	67,937,855 (GRCm38)	missense	probably benign
IGL02838:Vps13c	APN	9	67,975,851 (GRCm38)	missense	probably damaging	1.00
IGL03136:Vps13c	APN	9	67,950,310 (GRCm38)	missense	probably damaging	1.00
IGL03137:Vps13c	APN	9	67,890,380 (GRCm38)	missense	probably damaging	1.00
IGL03214:Vps13c	APN	9	67,897,195 (GRCm38)	missense	probably null	0.81
IGL03240:Vps13c	APN	9	67,955,047 (GRCm38)	missense	probably benign
IGL03303:Vps13c	APN	9	67,934,504 (GRCm38)	missense	probably benign	0.27
IGL03336:Vps13c	APN	9	67,951,642 (GRCm38)	missense	possibly damaging	0.76
IGL03366:Vps13c	APN	9	67,946,026 (GRCm38)	missense	probably benign	0.00
Derivative	UTSW	9	67,930,622 (GRCm38)	missense	possibly damaging	0.79
diversion	UTSW	9	67,910,233 (GRCm38)	missense	possibly damaging	0.93
introversion	UTSW	9	67,944,046 (GRCm38)	missense	probably damaging	0.98
Inversion	UTSW	9	67,902,839 (GRCm38)	critical splice acceptor site	probably null
subversion	UTSW	9	67,908,052 (GRCm38)	missense	probably damaging	1.00
Transversion	UTSW	9	67,934,501 (GRCm38)	missense	probably damaging	0.98
3-1:Vps13c	UTSW	9	67,936,373 (GRCm38)	missense	probably benign	0.00
IGL02991:Vps13c	UTSW	9	67,913,877 (GRCm38)	missense	probably damaging	1.00
PIT4802001:Vps13c	UTSW	9	67,937,786 (GRCm38)	missense	probably damaging	1.00
R0008:Vps13c	UTSW	9	67,919,262 (GRCm38)	missense	probably benign
R0206:Vps13c	UTSW	9	67,939,162 (GRCm38)	splice site	probably benign
R0288:Vps13c	UTSW	9	67,927,366 (GRCm38)	missense	probably damaging	0.99
R0324:Vps13c	UTSW	9	67,964,309 (GRCm38)	missense	possibly damaging	0.95
R0347:Vps13c	UTSW	9	67,910,233 (GRCm38)	missense	possibly damaging	0.93
R0374:Vps13c	UTSW	9	67,886,246 (GRCm38)	splice site	probably benign
R0388:Vps13c	UTSW	9	67,922,915 (GRCm38)	splice site	probably benign
R0409:Vps13c	UTSW	9	67,951,644 (GRCm38)	missense	probably benign	0.00
R0440:Vps13c	UTSW	9	67,972,861 (GRCm38)	missense	probably damaging	1.00
R0513:Vps13c	UTSW	9	67,930,735 (GRCm38)	missense	probably benign	0.02
R0520:Vps13c	UTSW	9	67,945,851 (GRCm38)	missense	possibly damaging	0.88
R0569:Vps13c	UTSW	9	67,973,719 (GRCm38)	missense	probably damaging	0.98
R0601:Vps13c	UTSW	9	67,927,472 (GRCm38)	missense	probably benign	0.12
R0659:Vps13c	UTSW	9	67,920,935 (GRCm38)	missense	probably benign	0.11
R0667:Vps13c	UTSW	9	67,951,573 (GRCm38)	nonsense	probably null
R0670:Vps13c	UTSW	9	67,925,857 (GRCm38)	missense	probably benign	0.35
R0698:Vps13c	UTSW	9	67,889,723 (GRCm38)	missense	probably benign	0.45
R0729:Vps13c	UTSW	9	67,961,649 (GRCm38)	missense	probably damaging	1.00
R0781:Vps13c	UTSW	9	67,972,003 (GRCm38)	missense	probably damaging	1.00
R0811:Vps13c	UTSW	9	67,934,476 (GRCm38)	missense	probably benign	0.06
R0812:Vps13c	UTSW	9	67,934,476 (GRCm38)	missense	probably benign	0.06
R0839:Vps13c	UTSW	9	67,898,738 (GRCm38)	missense	probably benign
R1373:Vps13c	UTSW	9	67,927,511 (GRCm38)	missense	probably damaging	0.99
R1499:Vps13c	UTSW	9	67,957,505 (GRCm38)	missense	probably benign	0.00
R1556:Vps13c	UTSW	9	67,930,711 (GRCm38)	missense	probably damaging	0.98
R1560:Vps13c	UTSW	9	67,936,463 (GRCm38)	critical splice donor site	probably null
R1584:Vps13c	UTSW	9	67,893,112 (GRCm38)	missense	possibly damaging	0.74
R1654:Vps13c	UTSW	9	67,951,687 (GRCm38)	missense	probably damaging	1.00
R1674:Vps13c	UTSW	9	67,853,703 (GRCm38)	nonsense	probably null
R1676:Vps13c	UTSW	9	67,926,962 (GRCm38)	missense	probably benign	0.20
R1695:Vps13c	UTSW	9	67,972,075 (GRCm38)	nonsense	probably null
R1710:Vps13c	UTSW	9	67,911,529 (GRCm38)	missense	probably benign	0.00
R1769:Vps13c	UTSW	9	67,965,721 (GRCm38)	missense	probably benign	0.00
R1775:Vps13c	UTSW	9	67,881,447 (GRCm38)	missense	probably damaging	1.00
R1795:Vps13c	UTSW	9	67,893,985 (GRCm38)	nonsense	probably null
R1799:Vps13c	UTSW	9	67,944,117 (GRCm38)	missense	probably damaging	0.98
R1835:Vps13c	UTSW	9	67,993,013 (GRCm38)	missense	probably benign	0.08
R1848:Vps13c	UTSW	9	67,936,340 (GRCm38)	missense	probably benign
R1903:Vps13c	UTSW	9	67,894,052 (GRCm38)	missense	probably damaging	1.00
R1944:Vps13c	UTSW	9	67,886,276 (GRCm38)	missense	probably damaging	1.00
R1945:Vps13c	UTSW	9	67,886,276 (GRCm38)	missense	probably damaging	1.00
R1951:Vps13c	UTSW	9	67,973,759 (GRCm38)	critical splice donor site	probably null
R1993:Vps13c	UTSW	9	67,975,856 (GRCm38)	missense	probably damaging	1.00
R2023:Vps13c	UTSW	9	67,936,285 (GRCm38)	splice site	probably benign
R2059:Vps13c	UTSW	9	67,860,833 (GRCm38)	missense	probably damaging	1.00
R2086:Vps13c	UTSW	9	67,950,289 (GRCm38)	missense	probably benign	0.29
R2120:Vps13c	UTSW	9	67,919,334 (GRCm38)	missense	possibly damaging	0.92
R2249:Vps13c	UTSW	9	67,988,053 (GRCm38)	critical splice donor site	probably null
R2257:Vps13c	UTSW	9	67,952,946 (GRCm38)	missense	possibly damaging	0.87
R2258:Vps13c	UTSW	9	67,953,860 (GRCm38)	missense	probably benign	0.01
R2259:Vps13c	UTSW	9	67,953,860 (GRCm38)	missense	probably benign	0.01
R2260:Vps13c	UTSW	9	67,953,860 (GRCm38)	missense	probably benign	0.01
R2265:Vps13c	UTSW	9	67,920,947 (GRCm38)	missense	possibly damaging	0.82
R2266:Vps13c	UTSW	9	67,920,947 (GRCm38)	missense	possibly damaging	0.82
R2269:Vps13c	UTSW	9	67,920,947 (GRCm38)	missense	possibly damaging	0.82
R2278:Vps13c	UTSW	9	67,939,072 (GRCm38)	missense	probably benign
R2306:Vps13c	UTSW	9	67,987,993 (GRCm38)	missense	probably damaging	0.99
R2327:Vps13c	UTSW	9	67,913,820 (GRCm38)	missense	probably damaging	0.98
R2349:Vps13c	UTSW	9	67,957,526 (GRCm38)	missense	possibly damaging	0.89
R2483:Vps13c	UTSW	9	67,975,907 (GRCm38)	critical splice donor site	probably null
R3031:Vps13c	UTSW	9	67,923,770 (GRCm38)	missense	probably benign	0.00
R3623:Vps13c	UTSW	9	67,975,907 (GRCm38)	critical splice donor site	probably null
R3870:Vps13c	UTSW	9	67,884,726 (GRCm38)	missense	probably benign	0.00
R4173:Vps13c	UTSW	9	67,936,313 (GRCm38)	missense	probably benign	0.00
R4445:Vps13c	UTSW	9	67,982,495 (GRCm38)	splice site	probably null
R4491:Vps13c	UTSW	9	67,910,193 (GRCm38)	missense	probably benign
R4505:Vps13c	UTSW	9	67,939,034 (GRCm38)	missense	probably benign	0.02
R4574:Vps13c	UTSW	9	67,951,683 (GRCm38)	missense	probably damaging	1.00
R4691:Vps13c	UTSW	9	67,952,935 (GRCm38)	missense	possibly damaging	0.95
R4766:Vps13c	UTSW	9	67,878,224 (GRCm38)	splice site	probably null
R4771:Vps13c	UTSW	9	67,929,539 (GRCm38)	missense	probably benign
R4801:Vps13c	UTSW	9	67,964,282 (GRCm38)	missense	probably damaging	1.00
R4802:Vps13c	UTSW	9	67,964,282 (GRCm38)	missense	probably damaging	1.00
R4962:Vps13c	UTSW	9	67,873,891 (GRCm38)	missense	probably damaging	1.00
R4995:Vps13c	UTSW	9	67,919,321 (GRCm38)	missense	probably benign	0.00
R5010:Vps13c	UTSW	9	67,916,379 (GRCm38)	missense	probably benign	0.19
R5183:Vps13c	UTSW	9	67,908,052 (GRCm38)	missense	probably damaging	1.00
R5226:Vps13c	UTSW	9	67,945,553 (GRCm38)	missense	probably benign	0.17
R5297:Vps13c	UTSW	9	67,878,131 (GRCm38)	missense	probably damaging	1.00
R5456:Vps13c	UTSW	9	67,927,447 (GRCm38)	missense	possibly damaging	0.53
R5494:Vps13c	UTSW	9	67,948,146 (GRCm38)	missense	probably benign	0.00
R5521:Vps13c	UTSW	9	67,951,439 (GRCm38)	missense	probably benign	0.08
R5524:Vps13c	UTSW	9	67,957,556 (GRCm38)	missense	probably damaging	1.00
R5685:Vps13c	UTSW	9	67,963,173 (GRCm38)	missense	possibly damaging	0.64
R5731:Vps13c	UTSW	9	67,895,379 (GRCm38)	missense	probably damaging	1.00
R5812:Vps13c	UTSW	9	67,982,495 (GRCm38)	splice site	probably benign
R5867:Vps13c	UTSW	9	67,982,622 (GRCm38)	splice site	probably null
R5893:Vps13c	UTSW	9	67,902,839 (GRCm38)	critical splice acceptor site	probably null
R5902:Vps13c	UTSW	9	67,934,447 (GRCm38)	missense	probably benign	0.00
R5957:Vps13c	UTSW	9	67,954,971 (GRCm38)	missense	probably damaging	1.00
R6076:Vps13c	UTSW	9	67,911,602 (GRCm38)	missense	probably damaging	1.00
R6187:Vps13c	UTSW	9	67,915,657 (GRCm38)	missense	probably damaging	1.00
R6268:Vps13c	UTSW	9	67,951,449 (GRCm38)	missense	probably benign	0.10
R6547:Vps13c	UTSW	9	67,973,365 (GRCm38)	missense	probably damaging	1.00
R6716:Vps13c	UTSW	9	67,951,467 (GRCm38)	missense	probably benign	0.00
R6837:Vps13c	UTSW	9	67,910,222 (GRCm38)	missense	probably benign
R6919:Vps13c	UTSW	9	67,927,452 (GRCm38)	missense	probably damaging	0.97
R7039:Vps13c	UTSW	9	67,937,763 (GRCm38)	missense	probably damaging	1.00
R7058:Vps13c	UTSW	9	67,923,828 (GRCm38)	missense	probably benign	0.39
R7082:Vps13c	UTSW	9	67,883,453 (GRCm38)	missense	probably damaging	1.00
R7195:Vps13c	UTSW	9	67,945,825 (GRCm38)	missense	possibly damaging	0.95
R7244:Vps13c	UTSW	9	67,889,804 (GRCm38)	missense	probably benign	0.00
R7300:Vps13c	UTSW	9	67,940,544 (GRCm38)	missense	probably benign	0.20
R7314:Vps13c	UTSW	9	67,943,340 (GRCm38)	splice site	probably null
R7352:Vps13c	UTSW	9	67,840,446 (GRCm38)	missense	possibly damaging	0.94
R7368:Vps13c	UTSW	9	67,914,073 (GRCm38)	missense	probably benign	0.23
R7411:Vps13c	UTSW	9	67,972,001 (GRCm38)	missense	probably damaging	0.98
R7497:Vps13c	UTSW	9	67,840,479 (GRCm38)	missense	probably damaging	1.00
R7516:Vps13c	UTSW	9	67,955,007 (GRCm38)	missense	possibly damaging	0.89
R7638:Vps13c	UTSW	9	67,945,509 (GRCm38)	missense	probably damaging	1.00
R7732:Vps13c	UTSW	9	67,940,516 (GRCm38)	missense	probably damaging	0.97
R7748:Vps13c	UTSW	9	67,963,089 (GRCm38)	missense	probably benign	0.03
R7779:Vps13c	UTSW	9	67,881,422 (GRCm38)	missense	probably damaging	1.00
R7788:Vps13c	UTSW	9	67,940,483 (GRCm38)	missense	probably benign	0.01
R7894:Vps13c	UTSW	9	67,926,983 (GRCm38)	missense	probably damaging	0.99
R8163:Vps13c	UTSW	9	67,950,438 (GRCm38)	missense	probably benign	0.08
R8165:Vps13c	UTSW	9	67,858,790 (GRCm38)	missense	probably benign	0.00
R8202:Vps13c	UTSW	9	67,944,046 (GRCm38)	missense	probably damaging	0.98
R8235:Vps13c	UTSW	9	67,955,781 (GRCm38)	missense	probably benign	0.01
R8235:Vps13c	UTSW	9	67,927,396 (GRCm38)	missense	probably damaging	1.00
R8253:Vps13c	UTSW	9	67,943,488 (GRCm38)	nonsense	probably null
R8261:Vps13c	UTSW	9	67,954,980 (GRCm38)	missense	probably damaging	1.00
R8348:Vps13c	UTSW	9	67,879,103 (GRCm38)	missense	possibly damaging	0.79
R8547:Vps13c	UTSW	9	67,945,566 (GRCm38)	missense	probably damaging	1.00
R8734:Vps13c	UTSW	9	67,973,403 (GRCm38)	missense	probably damaging	1.00
R8806:Vps13c	UTSW	9	67,945,828 (GRCm38)	missense	probably damaging	1.00
R8807:Vps13c	UTSW	9	67,858,840 (GRCm38)	missense	probably damaging	0.99
R8813:Vps13c	UTSW	9	67,871,284 (GRCm38)	missense	probably damaging	1.00
R8883:Vps13c	UTSW	9	67,948,197 (GRCm38)	missense	probably benign	0.10
R8885:Vps13c	UTSW	9	67,943,454 (GRCm38)	missense	probably benign
R8899:Vps13c	UTSW	9	67,934,501 (GRCm38)	missense	probably damaging	0.98
R8970:Vps13c	UTSW	9	67,945,521 (GRCm38)	missense	probably benign	0.11
R9007:Vps13c	UTSW	9	67,937,724 (GRCm38)	missense	probably benign	0.00
R9026:Vps13c	UTSW	9	67,954,581 (GRCm38)	missense	probably damaging	1.00
R9029:Vps13c	UTSW	9	67,948,147 (GRCm38)	missense	probably damaging	0.98
R9057:Vps13c	UTSW	9	67,920,927 (GRCm38)	missense	probably benign	0.00
R9105:Vps13c	UTSW	9	67,870,799 (GRCm38)	intron	probably benign
R9130:Vps13c	UTSW	9	67,929,523 (GRCm38)	missense	probably damaging	1.00
R9286:Vps13c	UTSW	9	67,972,921 (GRCm38)	missense	probably benign	0.00
R9338:Vps13c	UTSW	9	67,951,695 (GRCm38)	missense	probably damaging	1.00
R9432:Vps13c	UTSW	9	67,922,855 (GRCm38)	missense	probably benign	0.02
R9460:Vps13c	UTSW	9	67,930,622 (GRCm38)	missense	possibly damaging	0.79
R9464:Vps13c	UTSW	9	67,951,392 (GRCm38)	missense	probably damaging	1.00
R9561:Vps13c	UTSW	9	67,965,512 (GRCm38)	missense	probably damaging	1.00
R9609:Vps13c	UTSW	9	67,934,549 (GRCm38)	missense	probably damaging	1.00
R9622:Vps13c	UTSW	9	67,949,433 (GRCm38)	missense	probably damaging	1.00
R9665:Vps13c	UTSW	9	67,955,743 (GRCm38)	nonsense	probably null
R9731:Vps13c	UTSW	9	67,919,244 (GRCm38)	missense	probably benign
R9763:Vps13c	UTSW	9	67,911,578 (GRCm38)	missense	probably benign	0.00
R9774:Vps13c	UTSW	9	67,884,591 (GRCm38)	missense	possibly damaging	0.85
R9798:Vps13c	UTSW	9	67,919,364 (GRCm38)	missense	probably damaging	1.00
U24488:Vps13c	UTSW	9	67,905,916 (GRCm38)	missense	probably benign	0.13
X0021:Vps13c	UTSW	9	67,937,781 (GRCm38)	missense	probably damaging	0.99
X0058:Vps13c	UTSW	9	67,927,419 (GRCm38)	missense	probably damaging	1.00
X0065:Vps13c	UTSW	9	67,873,863 (GRCm38)	missense	probably damaging	1.00
Z1088:Vps13c	UTSW	9	67,913,975 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GAGCCAGAGCCAGTGAGAACTTTAG -3'
(R):5'- ACACGCATTTACAGGAACGGGG -3'

Sequencing Primer
(F):5'- GTGTTTGTAAAGCTGATTGAACGTG -3'
(R):5'- agcatctctttgtcccagttc -3'

Posted On

2014-03-17