Mutagenetix > Incidental Mutation

Incidental Mutation 'R6649:Cmya5'

527703

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E16Rik, 2310076E21Rik

MMRRC Submission

044770-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.299) question?

Stock #

R6649 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

93177221-93281232 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to C at 93234533 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Cysteine at position 185 (S185C)

Ref Sequence

ENSEMBL: ENSMUSP00000050408 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062122]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000062122
AA Change: S185C

PolyPhen 2 Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: S185C

Domain	Start	End	E-Value	Type
low complexity region	20	46	N/A	INTRINSIC
low complexity region	129	140	N/A	INTRINSIC
internal_repeat_1	448	535	5.09e-18	PROSPERO
internal_repeat_1	543	625	5.09e-18	PROSPERO
low complexity region	626	645	N/A	INTRINSIC
low complexity region	679	691	N/A	INTRINSIC
low complexity region	734	741	N/A	INTRINSIC
low complexity region	1001	1010	N/A	INTRINSIC
low complexity region	1166	1183	N/A	INTRINSIC
low complexity region	1259	1267	N/A	INTRINSIC
low complexity region	1440	1449	N/A	INTRINSIC
low complexity region	1876	1889	N/A	INTRINSIC
low complexity region	2632	2645	N/A	INTRINSIC
low complexity region	3048	3057	N/A	INTRINSIC
FN3	3312	3399	7.29e-4	SMART
FN3	3411	3492	1.3e0	SMART
Pfam:SPRY	3551	3668	6.7e-8	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224009

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.3%
20x: 95.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc2	T	A	19: 43,800,941 (GRCm39)	H627Q	probably benign	Het
Abra	G	A	15: 41,732,629 (GRCm39)	L146F	probably benign	Het
Adamts7	T	C	9: 90,073,990 (GRCm39)	C857R	probably damaging	Het
Ankhd1	A	T	18: 36,733,836 (GRCm39)		probably null	Het
Asb15	A	G	6: 24,562,632 (GRCm39)	N198S	probably benign	Het
Asb16	A	T	11: 102,159,863 (GRCm39)	Q72L	possibly damaging	Het
Atosa	T	G	9: 74,917,432 (GRCm39)	L677R	probably damaging	Het
Bbox1	G	T	2: 110,135,914 (GRCm39)	H22N	probably benign	Het
Bcdin3d	T	C	15: 99,368,696 (GRCm39)	T168A	probably damaging	Het
Bmp1	A	T	14: 70,728,058 (GRCm39)	W624R	probably damaging	Het
Cdh18	A	T	15: 23,436,620 (GRCm39)	Y492F	possibly damaging	Het
Cep290	A	C	10: 100,354,393 (GRCm39)	D848A	probably benign	Het
Cip2a	A	T	16: 48,837,829 (GRCm39)	Q843L	probably damaging	Het
Cops9	C	T	1: 92,568,136 (GRCm39)		probably benign	Het
Cutal	C	T	2: 34,775,933 (GRCm39)	T88I	probably benign	Het
Dlg4	G	T	11: 69,914,779 (GRCm39)		probably benign	Het
Dnah7c	C	A	1: 46,688,500 (GRCm39)	T1890K	probably benign	Het
Dnah7c	A	G	1: 46,688,511 (GRCm39)	S1894G	probably benign	Het
Eef2	CCC	CCCC	10: 81,014,602 (GRCm39)		probably null	Het
Erp44	T	C	4: 48,205,130 (GRCm39)	I288V	probably null	Het
Fat3	T	C	9: 16,288,038 (GRCm39)	D495G	probably damaging	Het
Fsip2	T	C	2: 82,798,161 (GRCm39)	V485A	possibly damaging	Het
Gm14496	A	T	2: 181,639,269 (GRCm39)	H453L	possibly damaging	Het
Gm17027	T	C	14: 41,981,236 (GRCm39)	T207A	unknown	Het
Gm6902	T	G	7: 22,973,159 (GRCm39)	T123P	possibly damaging	Het
Gpat2	T	G	2: 127,274,355 (GRCm39)	W366G	possibly damaging	Het
Heatr6	A	T	11: 83,650,191 (GRCm39)	T216S	probably benign	Het
Hsd17b14	T	C	7: 45,205,500 (GRCm39)	V11A	probably damaging	Het
Jak2	T	A	19: 29,266,110 (GRCm39)	I517N	probably benign	Het
Kmt5b	G	A	19: 3,857,295 (GRCm39)	G351R	probably damaging	Het
Mau2	G	T	8: 70,484,166 (GRCm39)	Q141K	possibly damaging	Het
Mfsd13a	T	C	19: 46,356,305 (GRCm39)	F137L	probably damaging	Het
Mfsd13a	A	G	19: 46,360,704 (GRCm39)	H394R	probably benign	Het
Mfsd14b	A	T	13: 65,214,599 (GRCm39)	I451N	probably damaging	Het
Milr1	C	T	11: 106,648,537 (GRCm39)	H143Y	probably benign	Het
Mon2	T	G	10: 122,874,385 (GRCm39)	K321T	possibly damaging	Het
Nlrp9c	T	A	7: 26,070,747 (GRCm39)	N945Y	probably damaging	Het
Nwd2	A	G	5: 63,882,527 (GRCm39)	R60G	possibly damaging	Het
Or2z2	A	T	11: 58,346,394 (GRCm39)	I127N	probably damaging	Het
Or52b2	T	C	7: 104,986,914 (GRCm39)	H3R	probably benign	Het
Or8g20	A	G	9: 39,396,048 (GRCm39)	V164A	probably benign	Het
Papola	A	T	12: 105,778,566 (GRCm39)	I315L	possibly damaging	Het
Phf3	A	T	1: 30,844,104 (GRCm39)	S1618R	possibly damaging	Het
Phyhipl	A	G	10: 70,404,843 (GRCm39)	F77L	probably damaging	Het
Ppp3cb	A	G	14: 20,581,094 (GRCm39)	L110P	probably damaging	Het
Prss53	T	G	7: 127,485,747 (GRCm39)	E531A	probably benign	Het
Raf1	A	T	6: 115,608,302 (GRCm39)	H236Q	probably benign	Het
Ryr2	A	G	13: 11,610,529 (GRCm39)	V4099A	probably damaging	Het
Sfxn3	G	A	19: 45,038,354 (GRCm39)		probably null	Het
Sh3pxd2b	T	C	11: 32,365,978 (GRCm39)		probably null	Het
Slco6c1	C	T	1: 97,053,436 (GRCm39)	S155N	probably benign	Het
Speer4f2	A	G	5: 17,580,767 (GRCm39)	T115A	probably benign	Het
Spry1	T	C	3: 37,696,871 (GRCm39)	I38T	probably damaging	Het
Tagap	T	C	17: 8,152,546 (GRCm39)	V577A	probably benign	Het
Ubr4	C	A	4: 139,200,935 (GRCm39)	H4706Q	possibly damaging	Het
Vmn2r112	T	A	17: 22,820,160 (GRCm39)	L11Q	probably null	Het
Zfp60	T	C	7: 27,448,151 (GRCm39)	F273S	probably benign	Het
Zfp938	A	T	10: 82,061,232 (GRCm39)	Y463N	probably damaging	Het

Other mutations in Cmya5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00489:Cmya5	APN	13	93,229,628 (GRCm39)	missense	probably benign	0.13
IGL00516:Cmya5	APN	13	93,234,675 (GRCm39)	missense	possibly damaging	0.73
IGL00654:Cmya5	APN	13	93,230,669 (GRCm39)	missense	probably benign	0.00
IGL00948:Cmya5	APN	13	93,227,544 (GRCm39)	missense	probably benign
IGL00966:Cmya5	APN	13	93,234,414 (GRCm39)	missense	probably benign	0.33
IGL00988:Cmya5	APN	13	93,234,441 (GRCm39)	missense	possibly damaging	0.96
IGL01106:Cmya5	APN	13	93,221,120 (GRCm39)	missense	probably damaging	1.00
IGL01331:Cmya5	APN	13	93,233,454 (GRCm39)	missense	possibly damaging	0.53
IGL01392:Cmya5	APN	13	93,225,714 (GRCm39)	missense	probably damaging	0.99
IGL01508:Cmya5	APN	13	93,230,535 (GRCm39)	missense	probably benign
IGL01679:Cmya5	APN	13	93,201,828 (GRCm39)	missense	probably damaging	1.00
IGL01749:Cmya5	APN	13	93,225,807 (GRCm39)	missense	probably benign	0.00
IGL01861:Cmya5	APN	13	93,226,256 (GRCm39)	missense	probably damaging	1.00
IGL02021:Cmya5	APN	13	93,231,057 (GRCm39)	missense	probably benign	0.00
IGL02034:Cmya5	APN	13	93,221,043 (GRCm39)	splice site	probably benign
IGL02103:Cmya5	APN	13	93,228,635 (GRCm39)	missense	probably benign	0.05
IGL02174:Cmya5	APN	13	93,185,415 (GRCm39)	missense	possibly damaging	0.76
IGL02176:Cmya5	APN	13	93,226,658 (GRCm39)	missense	probably damaging	1.00
IGL02210:Cmya5	APN	13	93,229,242 (GRCm39)	missense	probably benign	0.14
IGL02229:Cmya5	APN	13	93,229,194 (GRCm39)	missense	possibly damaging	0.54
IGL02306:Cmya5	APN	13	93,234,527 (GRCm39)	missense	probably damaging	1.00
IGL02311:Cmya5	APN	13	93,227,163 (GRCm39)	missense	probably benign	0.40
IGL02409:Cmya5	APN	13	93,226,706 (GRCm39)	missense	probably damaging	0.96
IGL02561:Cmya5	APN	13	93,228,366 (GRCm39)	missense	probably benign	0.00
IGL02676:Cmya5	APN	13	93,229,361 (GRCm39)	missense	probably damaging	1.00
IGL02683:Cmya5	APN	13	93,227,505 (GRCm39)	nonsense	probably null
IGL02685:Cmya5	APN	13	93,227,505 (GRCm39)	nonsense	probably null
IGL02686:Cmya5	APN	13	93,227,505 (GRCm39)	nonsense	probably null
IGL02724:Cmya5	APN	13	93,233,163 (GRCm39)	missense	probably benign
IGL02727:Cmya5	APN	13	93,234,753 (GRCm39)	missense	possibly damaging	0.73
IGL02965:Cmya5	APN	13	93,229,065 (GRCm39)	missense	probably benign	0.41
IGL03079:Cmya5	APN	13	93,234,209 (GRCm39)	missense	possibly damaging	0.85
IGL03144:Cmya5	APN	13	93,227,376 (GRCm39)	missense	probably damaging	1.00
IGL03253:Cmya5	APN	13	93,227,778 (GRCm39)	nonsense	probably null
IGL03336:Cmya5	APN	13	93,230,013 (GRCm39)	missense	possibly damaging	0.84
IGL03138:Cmya5	UTSW	13	93,201,850 (GRCm39)	missense	probably damaging	1.00
P0023:Cmya5	UTSW	13	93,225,854 (GRCm39)	missense	probably benign	0.22
P4748:Cmya5	UTSW	13	93,210,983 (GRCm39)	splice site	probably benign
R0123:Cmya5	UTSW	13	93,232,412 (GRCm39)	missense	possibly damaging	0.84
R0206:Cmya5	UTSW	13	93,232,065 (GRCm39)	missense	probably damaging	0.98
R0206:Cmya5	UTSW	13	93,232,065 (GRCm39)	missense	probably damaging	0.98
R0242:Cmya5	UTSW	13	93,232,108 (GRCm39)	missense	probably benign
R0242:Cmya5	UTSW	13	93,232,108 (GRCm39)	missense	probably benign
R0331:Cmya5	UTSW	13	93,280,911 (GRCm39)	missense	possibly damaging	0.53
R0363:Cmya5	UTSW	13	93,231,377 (GRCm39)	missense	possibly damaging	0.77
R0382:Cmya5	UTSW	13	93,229,256 (GRCm39)	missense	probably benign	0.06
R0416:Cmya5	UTSW	13	93,226,364 (GRCm39)	missense	probably benign	0.05
R0446:Cmya5	UTSW	13	93,230,164 (GRCm39)	missense	probably benign
R0457:Cmya5	UTSW	13	93,232,095 (GRCm39)	missense	possibly damaging	0.84
R0673:Cmya5	UTSW	13	93,226,505 (GRCm39)	missense	probably damaging	1.00
R0674:Cmya5	UTSW	13	93,229,299 (GRCm39)	missense	probably damaging	1.00
R0692:Cmya5	UTSW	13	93,230,357 (GRCm39)	nonsense	probably null
R0698:Cmya5	UTSW	13	93,232,065 (GRCm39)	missense	probably damaging	0.98
R1227:Cmya5	UTSW	13	93,230,954 (GRCm39)	missense	probably damaging	0.99
R1272:Cmya5	UTSW	13	93,231,620 (GRCm39)	missense	possibly damaging	0.79
R1335:Cmya5	UTSW	13	93,178,043 (GRCm39)	missense	possibly damaging	0.65
R1353:Cmya5	UTSW	13	93,178,033 (GRCm39)	missense	probably damaging	1.00
R1354:Cmya5	UTSW	13	93,228,566 (GRCm39)	missense	possibly damaging	0.46
R1458:Cmya5	UTSW	13	93,201,835 (GRCm39)	missense	probably benign	0.44
R1572:Cmya5	UTSW	13	93,230,777 (GRCm39)	missense	possibly damaging	0.61
R1698:Cmya5	UTSW	13	93,200,027 (GRCm39)	missense	probably benign	0.27
R1735:Cmya5	UTSW	13	93,226,297 (GRCm39)	missense	probably benign	0.11
R1743:Cmya5	UTSW	13	93,233,825 (GRCm39)	missense	probably benign	0.33
R1750:Cmya5	UTSW	13	93,232,171 (GRCm39)	missense	probably benign
R1827:Cmya5	UTSW	13	93,210,956 (GRCm39)	missense	possibly damaging	0.80
R2068:Cmya5	UTSW	13	93,227,032 (GRCm39)	missense	possibly damaging	0.93
R2088:Cmya5	UTSW	13	93,229,320 (GRCm39)	missense	probably damaging	1.00
R2132:Cmya5	UTSW	13	93,205,891 (GRCm39)	missense	probably damaging	1.00
R2216:Cmya5	UTSW	13	93,230,003 (GRCm39)	missense	probably damaging	1.00
R2363:Cmya5	UTSW	13	93,230,210 (GRCm39)	missense	probably benign	0.15
R2497:Cmya5	UTSW	13	93,234,513 (GRCm39)	missense	possibly damaging	0.53
R2509:Cmya5	UTSW	13	93,230,066 (GRCm39)	missense	probably benign	0.41
R2917:Cmya5	UTSW	13	93,227,572 (GRCm39)	nonsense	probably null
R2944:Cmya5	UTSW	13	93,229,350 (GRCm39)	nonsense	probably null
R3039:Cmya5	UTSW	13	93,228,758 (GRCm39)	missense	probably benign	0.12
R3078:Cmya5	UTSW	13	93,185,435 (GRCm39)	missense	probably damaging	0.99
R3708:Cmya5	UTSW	13	93,231,874 (GRCm39)	nonsense	probably null
R3717:Cmya5	UTSW	13	93,228,995 (GRCm39)	missense	probably benign	0.12
R3768:Cmya5	UTSW	13	93,233,201 (GRCm39)	missense	possibly damaging	0.73
R3769:Cmya5	UTSW	13	93,233,201 (GRCm39)	missense	possibly damaging	0.73
R3840:Cmya5	UTSW	13	93,231,140 (GRCm39)	missense	probably damaging	0.96
R3841:Cmya5	UTSW	13	93,231,140 (GRCm39)	missense	probably damaging	0.96
R3882:Cmya5	UTSW	13	93,227,727 (GRCm39)	missense	probably benign	0.07
R3888:Cmya5	UTSW	13	93,230,164 (GRCm39)	missense	probably benign
R3897:Cmya5	UTSW	13	93,233,189 (GRCm39)	missense	possibly damaging	0.72
R3952:Cmya5	UTSW	13	93,225,707 (GRCm39)	missense	possibly damaging	0.89
R4366:Cmya5	UTSW	13	93,228,464 (GRCm39)	missense	probably benign	0.36
R4471:Cmya5	UTSW	13	93,228,833 (GRCm39)	missense	probably benign	0.01
R4493:Cmya5	UTSW	13	93,230,573 (GRCm39)	missense	probably benign
R4495:Cmya5	UTSW	13	93,230,573 (GRCm39)	missense	probably benign
R4544:Cmya5	UTSW	13	93,228,426 (GRCm39)	nonsense	probably null
R4545:Cmya5	UTSW	13	93,228,426 (GRCm39)	nonsense	probably null
R4624:Cmya5	UTSW	13	93,200,059 (GRCm39)	missense	probably damaging	1.00
R4648:Cmya5	UTSW	13	93,230,336 (GRCm39)	missense	possibly damaging	0.84
R4824:Cmya5	UTSW	13	93,230,082 (GRCm39)	missense	probably benign	0.04
R4965:Cmya5	UTSW	13	93,232,295 (GRCm39)	missense	possibly damaging	0.84
R4967:Cmya5	UTSW	13	93,227,093 (GRCm39)	missense	probably damaging	1.00
R5101:Cmya5	UTSW	13	93,228,111 (GRCm39)	missense	possibly damaging	0.61
R5133:Cmya5	UTSW	13	93,229,880 (GRCm39)	missense	possibly damaging	0.79
R5139:Cmya5	UTSW	13	93,232,569 (GRCm39)	missense	probably benign	0.00
R5220:Cmya5	UTSW	13	93,228,804 (GRCm39)	missense	probably damaging	0.99
R5332:Cmya5	UTSW	13	93,232,703 (GRCm39)	missense	probably damaging	0.96
R5337:Cmya5	UTSW	13	93,219,781 (GRCm39)	missense	probably benign	0.28
R5356:Cmya5	UTSW	13	93,199,993 (GRCm39)	missense	probably damaging	1.00
R5401:Cmya5	UTSW	13	93,228,476 (GRCm39)	missense	probably damaging	1.00
R5438:Cmya5	UTSW	13	93,231,707 (GRCm39)	missense	possibly damaging	0.89
R5604:Cmya5	UTSW	13	93,229,271 (GRCm39)	missense	probably benign	0.15
R5628:Cmya5	UTSW	13	93,226,218 (GRCm39)	missense	probably damaging	1.00
R5666:Cmya5	UTSW	13	93,182,457 (GRCm39)	missense	possibly damaging	0.75
R5687:Cmya5	UTSW	13	93,234,684 (GRCm39)	missense	possibly damaging	0.53
R5695:Cmya5	UTSW	13	93,182,374 (GRCm39)	critical splice donor site	probably null
R5806:Cmya5	UTSW	13	93,230,445 (GRCm39)	missense	possibly damaging	0.84
R5820:Cmya5	UTSW	13	93,229,288 (GRCm39)	missense	probably benign	0.04
R5872:Cmya5	UTSW	13	93,233,943 (GRCm39)	missense	probably benign	0.01
R5875:Cmya5	UTSW	13	93,231,692 (GRCm39)	missense	probably benign	0.13
R5896:Cmya5	UTSW	13	93,182,373 (GRCm39)	critical splice donor site	probably null
R5910:Cmya5	UTSW	13	93,229,151 (GRCm39)	missense	probably damaging	0.98
R5969:Cmya5	UTSW	13	93,226,052 (GRCm39)	missense	possibly damaging	0.78
R6064:Cmya5	UTSW	13	93,226,157 (GRCm39)	missense	probably damaging	1.00
R6081:Cmya5	UTSW	13	93,281,021 (GRCm39)	unclassified	probably benign
R6102:Cmya5	UTSW	13	93,230,739 (GRCm39)	missense	probably benign
R6117:Cmya5	UTSW	13	93,231,674 (GRCm39)	missense	probably damaging	0.98
R6188:Cmya5	UTSW	13	93,233,784 (GRCm39)	missense	possibly damaging	0.73
R6188:Cmya5	UTSW	13	93,229,952 (GRCm39)	missense	possibly damaging	0.61
R6219:Cmya5	UTSW	13	93,230,951 (GRCm39)	missense	probably damaging	1.00
R6229:Cmya5	UTSW	13	93,229,814 (GRCm39)	missense	probably benign	0.41
R6346:Cmya5	UTSW	13	93,228,698 (GRCm39)	missense	probably damaging	1.00
R6431:Cmya5	UTSW	13	93,210,972 (GRCm39)	missense	possibly damaging	0.60
R6436:Cmya5	UTSW	13	93,225,723 (GRCm39)	missense	probably damaging	0.98
R6598:Cmya5	UTSW	13	93,226,316 (GRCm39)	missense	probably benign	0.05
R6652:Cmya5	UTSW	13	93,229,547 (GRCm39)	missense	probably damaging	0.99
R6652:Cmya5	UTSW	13	93,229,403 (GRCm39)	missense	probably benign	0.04
R6669:Cmya5	UTSW	13	93,229,767 (GRCm39)	missense	probably benign	0.03
R6881:Cmya5	UTSW	13	93,226,800 (GRCm39)	missense	probably damaging	1.00
R6909:Cmya5	UTSW	13	93,227,760 (GRCm39)	missense	probably benign	0.04
R6933:Cmya5	UTSW	13	93,231,644 (GRCm39)	missense	probably benign	0.03
R7021:Cmya5	UTSW	13	93,230,063 (GRCm39)	missense	possibly damaging	0.62
R7022:Cmya5	UTSW	13	93,205,786 (GRCm39)	critical splice donor site	probably null
R7068:Cmya5	UTSW	13	93,229,205 (GRCm39)	missense	possibly damaging	0.59
R7087:Cmya5	UTSW	13	93,227,483 (GRCm39)	missense	probably benign	0.00
R7088:Cmya5	UTSW	13	93,228,372 (GRCm39)	missense	possibly damaging	0.95
R7126:Cmya5	UTSW	13	93,226,448 (GRCm39)	missense	probably benign	0.41
R7177:Cmya5	UTSW	13	93,231,836 (GRCm39)	missense	probably benign	0.00
R7188:Cmya5	UTSW	13	93,182,546 (GRCm39)	missense	probably damaging	1.00
R7217:Cmya5	UTSW	13	93,226,938 (GRCm39)	missense	probably damaging	1.00
R7278:Cmya5	UTSW	13	93,232,208 (GRCm39)	missense	probably damaging	0.96
R7293:Cmya5	UTSW	13	93,229,305 (GRCm39)	missense	possibly damaging	0.90
R7332:Cmya5	UTSW	13	93,229,061 (GRCm39)	missense	possibly damaging	0.60
R7375:Cmya5	UTSW	13	93,228,169 (GRCm39)	missense	probably damaging	0.97
R7386:Cmya5	UTSW	13	93,205,831 (GRCm39)	missense	probably damaging	1.00
R7489:Cmya5	UTSW	13	93,228,346 (GRCm39)	missense	possibly damaging	0.87
R7529:Cmya5	UTSW	13	93,233,942 (GRCm39)	missense	probably benign	0.02
R7552:Cmya5	UTSW	13	93,205,820 (GRCm39)	missense	probably benign	0.41
R7624:Cmya5	UTSW	13	93,226,865 (GRCm39)	missense	possibly damaging	0.79
R7637:Cmya5	UTSW	13	93,219,720 (GRCm39)	missense	possibly damaging	0.87
R7673:Cmya5	UTSW	13	93,230,629 (GRCm39)	missense	probably benign	0.13
R7753:Cmya5	UTSW	13	93,234,680 (GRCm39)	missense	probably benign	0.18
R7757:Cmya5	UTSW	13	93,234,780 (GRCm39)	missense	possibly damaging	0.53
R7806:Cmya5	UTSW	13	93,230,770 (GRCm39)	missense	probably benign	0.00
R7825:Cmya5	UTSW	13	93,234,136 (GRCm39)	missense	possibly damaging	0.53
R7878:Cmya5	UTSW	13	93,226,265 (GRCm39)	missense	probably damaging	0.98
R7892:Cmya5	UTSW	13	93,232,865 (GRCm39)	missense	probably damaging	0.96
R7952:Cmya5	UTSW	13	93,233,512 (GRCm39)	small deletion	probably benign
R8127:Cmya5	UTSW	13	93,231,122 (GRCm39)	missense	probably damaging	0.99
R8256:Cmya5	UTSW	13	93,229,986 (GRCm39)	missense	possibly damaging	0.62
R8339:Cmya5	UTSW	13	93,228,142 (GRCm39)	nonsense	probably null
R8446:Cmya5	UTSW	13	93,230,336 (GRCm39)	missense	possibly damaging	0.84
R8553:Cmya5	UTSW	13	93,230,304 (GRCm39)	missense	probably benign	0.00
R8686:Cmya5	UTSW	13	93,231,888 (GRCm39)	missense	possibly damaging	0.91
R8748:Cmya5	UTSW	13	93,226,229 (GRCm39)	missense	probably damaging	1.00
R8783:Cmya5	UTSW	13	93,225,888 (GRCm39)	missense	possibly damaging	0.58
R8803:Cmya5	UTSW	13	93,177,991 (GRCm39)	missense	probably damaging	1.00
R8810:Cmya5	UTSW	13	93,200,048 (GRCm39)	missense	possibly damaging	0.47
R8937:Cmya5	UTSW	13	93,232,840 (GRCm39)	missense	probably benign	0.01
R8985:Cmya5	UTSW	13	93,233,664 (GRCm39)	missense	possibly damaging	0.73
R9017:Cmya5	UTSW	13	93,228,572 (GRCm39)	missense	probably benign	0.03
R9087:Cmya5	UTSW	13	93,233,711 (GRCm39)	missense	possibly damaging	0.72
R9133:Cmya5	UTSW	13	93,234,108 (GRCm39)	missense	possibly damaging	0.73
R9156:Cmya5	UTSW	13	93,233,878 (GRCm39)	missense	unknown
R9209:Cmya5	UTSW	13	93,226,866 (GRCm39)	missense	probably benign	0.45
R9222:Cmya5	UTSW	13	93,230,579 (GRCm39)	missense	probably benign	0.00
R9229:Cmya5	UTSW	13	93,232,176 (GRCm39)	missense	possibly damaging	0.92
R9382:Cmya5	UTSW	13	93,229,884 (GRCm39)	missense	probably benign
R9385:Cmya5	UTSW	13	93,230,880 (GRCm39)	missense	probably damaging	0.99
R9418:Cmya5	UTSW	13	93,226,209 (GRCm39)	missense	probably benign	0.22
R9452:Cmya5	UTSW	13	93,232,394 (GRCm39)	missense	probably benign
R9492:Cmya5	UTSW	13	93,177,822 (GRCm39)	makesense	probably null
R9600:Cmya5	UTSW	13	93,226,604 (GRCm39)	missense	probably damaging	1.00
R9712:Cmya5	UTSW	13	93,201,881 (GRCm39)	critical splice acceptor site	probably null
R9742:Cmya5	UTSW	13	93,231,935 (GRCm39)	missense	possibly damaging	0.89
RF020:Cmya5	UTSW	13	93,205,799 (GRCm39)	missense	possibly damaging	0.56
X0028:Cmya5	UTSW	13	93,233,195 (GRCm39)	missense	possibly damaging	0.53
Z1088:Cmya5	UTSW	13	93,200,087 (GRCm39)	missense	probably benign
Z1176:Cmya5	UTSW	13	93,233,298 (GRCm39)	missense	unknown
Z1176:Cmya5	UTSW	13	93,200,087 (GRCm39)	missense	probably benign
Z1177:Cmya5	UTSW	13	93,200,087 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GGCAACGTCCCATAAAATTGTAGAG -3'
(R):5'- CTGACTTCTCCTCCAGGAAGTG -3'

Sequencing Primer
(F):5'- GTTCCTATGTAGACTGGCT -3'
(R):5'- TTATGGATGAAGTTAAAAGGACACG -3'

Posted On

2018-07-23