Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02017:Lama1'

183792

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Lama1

Ensembl Gene

ENSMUSG00000032796

Gene Name

laminin, alpha 1

Synonyms

Lama

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL02017

Quality Score

Status

Chromosome

Chromosomal Location

67697265-67822645 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 67764725 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 869 (H869R)

Ref Sequence

ENSEMBL: ENSMUSP00000043957 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035471]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000035471
AA Change: H869R

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

SMART Domains

Protein: ENSMUSP00000043957
Gene: ENSMUSG00000032796
AA Change: H869R

Domain	Start	End	E-Value	Type
low complexity region	3	22	N/A	INTRINSIC
LamNT	23	275	1.2e-131	SMART
EGF_Lam	277	331	1e-5	SMART
EGF_Lam	334	401	6.6e-6	SMART
EGF_Lam	404	458	9.11e-9	SMART
EGF_Lam	461	507	8.12e-6	SMART
LamB	570	702	2.09e-57	SMART
EGF_like	715	746	3.36e0	SMART
EGF_Lam	749	795	7.01e-10	SMART
EGF_Lam	798	853	3.59e-7	SMART
EGF_Lam	856	906	1.53e-10	SMART
EGF_Lam	909	955	1.13e-13	SMART
EGF_Lam	958	1002	1.36e-7	SMART
EGF_Lam	1005	1048	7.29e-8	SMART
EGF_like	1034	1082	4.83e1	SMART
EGF_Lam	1051	1094	1.67e-7	SMART
EGF_Lam	1097	1154	1.32e-5	SMART
LamB	1220	1352	8.7e-46	SMART
Pfam:Laminin_EGF	1367	1397	1.7e-6	PFAM
EGF_Lam	1410	1456	7.12e-11	SMART
EGF_Lam	1459	1513	3.25e-5	SMART
EGF_like	1497	1547	6.41e1	SMART
EGF_Lam	1516	1560	1.71e-13	SMART
Pfam:Laminin_I	1574	1838	1.7e-91	PFAM
low complexity region	2012	2031	N/A	INTRINSIC
low complexity region	2087	2098	N/A	INTRINSIC
LamG	2145	2287	3.66e-30	SMART
LamG	2332	2473	5.98e-35	SMART
LamG	2513	2661	1.11e-29	SMART
low complexity region	2695	2708	N/A	INTRINSIC
LamG	2743	2877	9.72e-35	SMART
LamG	2920	3056	4.63e-41	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the alpha 1 subunits of laminin. The laminins are a family of extracellular matrix glycoproteins that have a heterotrimeric structure consisting of an alpha, beta and gamma chain. These proteins make up a major component of the basement membrane and have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Mutations in this gene may be associated with Poretti-Boltshauser syndrome. [provided by RefSeq, Sep 2014]
PHENOTYPE: Homozygous null mice display embryonic lethality before somite formation with impaired formation of Reichert's membrane. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam5	A	T	8: 24,781,759 (GRCm38)	I544N	probably benign	Het
Ago2	T	C	15: 73,126,517 (GRCm38)	T271A	probably benign	Het
Aox3	A	C	1: 58,120,992 (GRCm38)	K111N	probably damaging	Het
Arhgap39	G	A	15: 76,737,037 (GRCm38)	R455C	probably damaging	Het
Brcc3	A	G	X: 75,422,783 (GRCm38)	D67G	possibly damaging	Het
Crot	T	G	5: 8,970,046 (GRCm38)		probably benign	Het
Dipk1c	A	T	18: 84,736,825 (GRCm38)	D142V	probably damaging	Het
Dusp5	A	G	19: 53,537,506 (GRCm38)	H193R	probably damaging	Het
Ect2	G	A	3: 27,122,044 (GRCm38)	R644*	probably null	Het
Epn3	A	G	11: 94,495,026 (GRCm38)	S190P	probably benign	Het
Fam3c	A	G	6: 22,343,277 (GRCm38)	M1T	probably null	Het
Kif4	A	G	X: 100,638,354 (GRCm38)	N197S	probably benign	Het
Krt2	T	C	15: 101,816,504 (GRCm38)	N224D	probably damaging	Het
Lrrc14	G	T	15: 76,713,742 (GRCm38)	R224L	probably damaging	Het
Macf1	T	C	4: 123,499,931 (GRCm38)	D864G	probably damaging	Het
Map3k11	C	T	19: 5,697,623 (GRCm38)	S603F	possibly damaging	Het
Mxra7	A	G	11: 116,811,921 (GRCm38)		probably null	Het
Myo5b	C	A	18: 74,716,999 (GRCm38)	D1139E	probably damaging	Het
Nek9	T	C	12: 85,329,923 (GRCm38)	Y228C	probably damaging	Het
Nxph1	T	C	6: 9,247,743 (GRCm38)	I238T	probably damaging	Het
Or2r11	T	C	6: 42,460,824 (GRCm38)	H65R	probably benign	Het
Or5ac17	A	G	16: 59,215,947 (GRCm38)	L222P	probably damaging	Het
Or9i1	T	A	19: 13,862,231 (GRCm38)	V146E	possibly damaging	Het
Pdpn	A	G	4: 143,270,570 (GRCm38)		probably benign	Het
Plbd2	T	C	5: 120,488,558 (GRCm38)	T329A	probably damaging	Het
Ptpn6	T	C	6: 124,732,486 (GRCm38)	D8G	probably damaging	Het
Rad54l2	T	C	9: 106,754,040 (GRCm38)	D16G	possibly damaging	Het
Slc43a3	A	G	2: 84,938,241 (GRCm38)	E68G	probably damaging	Het
Snph	G	A	2: 151,600,982 (GRCm38)	R16C	probably damaging	Het
Ttn	G	A	2: 76,725,216 (GRCm38)	R28736*	probably null	Het
Vmn1r18	G	A	6: 57,389,756 (GRCm38)	A271V	probably benign	Het

Other mutations in Lama1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00157:Lama1	APN	17	67,815,928 (GRCm38)	missense	probably benign
IGL00336:Lama1	APN	17	67,813,948 (GRCm38)	missense	probably benign	0.07
IGL01066:Lama1	APN	17	67,743,326 (GRCm38)	missense	probably damaging	1.00
IGL01140:Lama1	APN	17	67,802,933 (GRCm38)	missense	probably benign	0.14
IGL01291:Lama1	APN	17	67,738,870 (GRCm38)	missense	probably damaging	1.00
IGL01296:Lama1	APN	17	67,745,051 (GRCm38)	missense	probably benign	0.27
IGL01317:Lama1	APN	17	67,818,701 (GRCm38)	missense	probably damaging	1.00
IGL01490:Lama1	APN	17	67,750,584 (GRCm38)	missense	possibly damaging	0.54
IGL01506:Lama1	APN	17	67,785,070 (GRCm38)	missense	probably benign	0.01
IGL01508:Lama1	APN	17	67,809,361 (GRCm38)	splice site	probably benign
IGL01522:Lama1	APN	17	67,752,774 (GRCm38)	splice site	probably benign
IGL01530:Lama1	APN	17	67,796,790 (GRCm38)	missense	probably benign	0.02
IGL01541:Lama1	APN	17	67,785,070 (GRCm38)	missense	probably benign	0.01
IGL01677:Lama1	APN	17	67,779,148 (GRCm38)	missense	probably benign	0.15
IGL01886:Lama1	APN	17	67,807,797 (GRCm38)	missense	probably benign	0.36
IGL01994:Lama1	APN	17	67,752,439 (GRCm38)	missense	probably benign	0.05
IGL02021:Lama1	APN	17	67,821,626 (GRCm38)	missense	probably damaging	1.00
IGL02026:Lama1	APN	17	67,809,292 (GRCm38)	missense	possibly damaging	0.82
IGL02044:Lama1	APN	17	67,811,490 (GRCm38)	missense	probably benign	0.01
IGL02120:Lama1	APN	17	67,716,789 (GRCm38)	missense	probably damaging	1.00
IGL02425:Lama1	APN	17	67,811,485 (GRCm38)	missense	probably benign	0.45
IGL02549:Lama1	APN	17	67,790,835 (GRCm38)	missense	possibly damaging	0.93
IGL02642:Lama1	APN	17	67,812,366 (GRCm38)	missense	probably benign	0.00
IGL02795:Lama1	APN	17	67,738,894 (GRCm38)	splice site	probably null
IGL02798:Lama1	APN	17	67,795,191 (GRCm38)	splice site	probably benign
IGL02863:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
IGL02870:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
IGL02876:Lama1	APN	17	67,750,692 (GRCm38)	critical splice donor site	probably null
IGL02885:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
IGL02891:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
IGL02978:Lama1	APN	17	67,786,081 (GRCm38)	nonsense	probably null
IGL03064:Lama1	APN	17	67,779,104 (GRCm38)	missense	probably benign	0.01
IGL03076:Lama1	APN	17	67,716,799 (GRCm38)	missense	possibly damaging	0.95
IGL03110:Lama1	APN	17	67,798,986 (GRCm38)	missense	probably benign	0.04
IGL03143:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
IGL03159:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
IGL03268:Lama1	APN	17	67,804,536 (GRCm38)	missense	probably damaging	0.99
ANU05:Lama1	UTSW	17	67,738,870 (GRCm38)	missense	probably damaging	1.00
PIT4472001:Lama1	UTSW	17	67,764,704 (GRCm38)	missense
R0047:Lama1	UTSW	17	67,795,186 (GRCm38)	splice site	probably benign
R0047:Lama1	UTSW	17	67,795,186 (GRCm38)	splice site	probably benign
R0050:Lama1	UTSW	17	67,782,056 (GRCm38)	missense	possibly damaging	0.66
R0096:Lama1	UTSW	17	67,805,413 (GRCm38)	missense	probably benign	0.12
R0096:Lama1	UTSW	17	67,805,413 (GRCm38)	missense	probably benign	0.12
R0111:Lama1	UTSW	17	67,737,498 (GRCm38)	missense	probably damaging	0.98
R0116:Lama1	UTSW	17	67,776,923 (GRCm38)	missense	probably benign	0.10
R0121:Lama1	UTSW	17	67,798,513 (GRCm38)	splice site	probably benign
R0278:Lama1	UTSW	17	67,810,183 (GRCm38)	missense	probably null	0.98
R0281:Lama1	UTSW	17	67,817,569 (GRCm38)	missense	probably damaging	1.00
R0312:Lama1	UTSW	17	67,775,851 (GRCm38)	missense	possibly damaging	0.45
R0419:Lama1	UTSW	17	67,791,610 (GRCm38)	critical splice donor site	probably null
R0512:Lama1	UTSW	17	67,779,134 (GRCm38)	missense	possibly damaging	0.67
R0514:Lama1	UTSW	17	67,764,698 (GRCm38)	missense	probably benign	0.40
R0562:Lama1	UTSW	17	67,815,959 (GRCm38)	missense	probably damaging	1.00
R0632:Lama1	UTSW	17	67,752,368 (GRCm38)	splice site	probably benign
R0645:Lama1	UTSW	17	67,773,712 (GRCm38)	missense	probably benign	0.01
R0712:Lama1	UTSW	17	67,779,042 (GRCm38)	splice site	probably null
R0763:Lama1	UTSW	17	67,772,818 (GRCm38)	missense	probably damaging	0.97
R0941:Lama1	UTSW	17	67,775,865 (GRCm38)	missense	probably benign	0.10
R1025:Lama1	UTSW	17	67,752,898 (GRCm38)	missense	probably benign	0.00
R1084:Lama1	UTSW	17	67,804,469 (GRCm38)	missense	probably benign	0.12
R1103:Lama1	UTSW	17	67,790,947 (GRCm38)	missense	probably damaging	0.98
R1420:Lama1	UTSW	17	67,790,947 (GRCm38)	missense	probably damaging	0.98
R1430:Lama1	UTSW	17	67,782,155 (GRCm38)	missense	possibly damaging	0.95
R1569:Lama1	UTSW	17	67,780,618 (GRCm38)	splice site	probably null
R1575:Lama1	UTSW	17	67,810,409 (GRCm38)	missense	possibly damaging	0.96
R1613:Lama1	UTSW	17	67,807,923 (GRCm38)	missense	probably benign	0.42
R1620:Lama1	UTSW	17	67,767,033 (GRCm38)	missense	probably benign	0.01
R1629:Lama1	UTSW	17	67,805,428 (GRCm38)	missense	probably benign	0.00
R1645:Lama1	UTSW	17	67,737,682 (GRCm38)	missense	probably benign	0.14
R1652:Lama1	UTSW	17	67,807,846 (GRCm38)	missense	probably damaging	0.97
R1674:Lama1	UTSW	17	67,791,244 (GRCm38)	missense	probably benign
R1678:Lama1	UTSW	17	67,810,155 (GRCm38)	missense	possibly damaging	0.56
R1710:Lama1	UTSW	17	67,753,791 (GRCm38)	missense	probably benign	0.00
R1712:Lama1	UTSW	17	67,717,186 (GRCm38)	missense	possibly damaging	0.95
R1737:Lama1	UTSW	17	67,802,921 (GRCm38)	missense	probably benign	0.36
R1757:Lama1	UTSW	17	67,697,383 (GRCm38)	missense	unknown
R1757:Lama1	UTSW	17	67,763,836 (GRCm38)	missense	probably benign	0.40
R1813:Lama1	UTSW	17	67,791,223 (GRCm38)	missense	probably benign
R1896:Lama1	UTSW	17	67,791,223 (GRCm38)	missense	probably benign
R1945:Lama1	UTSW	17	67,745,853 (GRCm38)	missense	probably benign	0.14
R2086:Lama1	UTSW	17	67,817,623 (GRCm38)	missense	probably damaging	1.00
R2149:Lama1	UTSW	17	67,773,865 (GRCm38)	missense	possibly damaging	0.95
R2178:Lama1	UTSW	17	67,769,515 (GRCm38)	missense	probably benign	0.07
R2183:Lama1	UTSW	17	67,791,009 (GRCm38)	missense	probably damaging	0.98
R2197:Lama1	UTSW	17	67,752,941 (GRCm38)	missense	probably benign	0.02
R2213:Lama1	UTSW	17	67,777,034 (GRCm38)	nonsense	probably null
R2260:Lama1	UTSW	17	67,737,507 (GRCm38)	missense	probably damaging	0.96
R2356:Lama1	UTSW	17	67,810,114 (GRCm38)	missense	probably damaging	1.00
R2420:Lama1	UTSW	17	67,750,553 (GRCm38)	missense	probably benign	0.00
R2421:Lama1	UTSW	17	67,750,553 (GRCm38)	missense	probably benign	0.00
R2422:Lama1	UTSW	17	67,750,553 (GRCm38)	missense	probably benign	0.00
R2424:Lama1	UTSW	17	67,798,665 (GRCm38)	missense	probably benign	0.09
R2442:Lama1	UTSW	17	67,768,317 (GRCm38)	missense	probably benign	0.04
R3147:Lama1	UTSW	17	67,737,658 (GRCm38)	missense	probably damaging	0.98
R3414:Lama1	UTSW	17	67,737,603 (GRCm38)	missense	probably damaging	1.00
R3683:Lama1	UTSW	17	67,768,333 (GRCm38)	missense	probably benign	0.40
R3820:Lama1	UTSW	17	67,779,046 (GRCm38)	splice site	probably null
R3821:Lama1	UTSW	17	67,779,046 (GRCm38)	splice site	probably null
R3822:Lama1	UTSW	17	67,779,046 (GRCm38)	splice site	probably null
R4012:Lama1	UTSW	17	67,812,373 (GRCm38)	nonsense	probably null
R4113:Lama1	UTSW	17	67,764,703 (GRCm38)	missense	probably benign	0.01
R4133:Lama1	UTSW	17	67,812,486 (GRCm38)	missense	probably damaging	1.00
R4133:Lama1	UTSW	17	67,750,655 (GRCm38)	missense	probably damaging	0.98
R4259:Lama1	UTSW	17	67,752,418 (GRCm38)	missense	possibly damaging	0.95
R4278:Lama1	UTSW	17	67,791,517 (GRCm38)	missense	probably null	0.00
R4321:Lama1	UTSW	17	67,771,083 (GRCm38)	missense	probably benign	0.03
R4374:Lama1	UTSW	17	67,804,518 (GRCm38)	missense	probably benign	0.00
R4386:Lama1	UTSW	17	67,773,712 (GRCm38)	missense	probably benign	0.01
R4463:Lama1	UTSW	17	67,761,700 (GRCm38)	missense	probably damaging	1.00
R4629:Lama1	UTSW	17	67,805,360 (GRCm38)	critical splice acceptor site	probably null
R4630:Lama1	UTSW	17	67,794,300 (GRCm38)	missense	probably benign	0.00
R4633:Lama1	UTSW	17	67,798,584 (GRCm38)	missense	probably damaging	0.96
R4668:Lama1	UTSW	17	67,752,434 (GRCm38)	missense	probably benign	0.27
R4684:Lama1	UTSW	17	67,773,778 (GRCm38)	missense	possibly damaging	0.88
R4745:Lama1	UTSW	17	67,738,780 (GRCm38)	missense	probably damaging	1.00
R4786:Lama1	UTSW	17	67,773,859 (GRCm38)	missense	possibly damaging	0.77
R4797:Lama1	UTSW	17	67,716,775 (GRCm38)	missense	probably benign	0.04
R4803:Lama1	UTSW	17	67,809,271 (GRCm38)	missense	probably damaging	1.00
R4925:Lama1	UTSW	17	67,794,314 (GRCm38)	missense	probably benign	0.02
R4939:Lama1	UTSW	17	67,737,475 (GRCm38)	missense	possibly damaging	0.91
R4952:Lama1	UTSW	17	67,767,566 (GRCm38)	critical splice donor site	probably null
R4975:Lama1	UTSW	17	67,738,834 (GRCm38)	missense	possibly damaging	0.95
R4977:Lama1	UTSW	17	67,737,682 (GRCm38)	missense	probably damaging	1.00
R5039:Lama1	UTSW	17	67,745,893 (GRCm38)	missense	possibly damaging	0.66
R5047:Lama1	UTSW	17	67,743,281 (GRCm38)	nonsense	probably null
R5195:Lama1	UTSW	17	67,764,800 (GRCm38)	missense	probably benign	0.13
R5230:Lama1	UTSW	17	67,745,083 (GRCm38)	nonsense	probably null
R5236:Lama1	UTSW	17	67,804,492 (GRCm38)	missense	probably benign	0.24
R5254:Lama1	UTSW	17	67,756,716 (GRCm38)	missense	probably benign	0.01
R5345:Lama1	UTSW	17	67,817,563 (GRCm38)	missense	probably benign
R5438:Lama1	UTSW	17	67,800,774 (GRCm38)	missense	possibly damaging	0.92
R5521:Lama1	UTSW	17	67,780,894 (GRCm38)	nonsense	probably null
R5568:Lama1	UTSW	17	67,768,298 (GRCm38)	critical splice acceptor site	probably null
R5645:Lama1	UTSW	17	67,802,948 (GRCm38)	missense	probably damaging	1.00
R5665:Lama1	UTSW	17	67,770,987 (GRCm38)	missense	probably damaging	1.00
R5727:Lama1	UTSW	17	67,815,224 (GRCm38)	missense	possibly damaging	0.81
R5757:Lama1	UTSW	17	67,738,787 (GRCm38)	missense	possibly damaging	0.59
R5795:Lama1	UTSW	17	67,796,727 (GRCm38)	missense	probably benign	0.02
R5857:Lama1	UTSW	17	67,807,843 (GRCm38)	missense	probably damaging	0.99
R5894:Lama1	UTSW	17	67,779,047 (GRCm38)	critical splice acceptor site	probably null
R5974:Lama1	UTSW	17	67,773,727 (GRCm38)	missense	probably benign	0.31
R6032:Lama1	UTSW	17	67,750,643 (GRCm38)	missense	probably benign	0.01
R6032:Lama1	UTSW	17	67,750,643 (GRCm38)	missense	probably benign	0.01
R6120:Lama1	UTSW	17	67,780,617 (GRCm38)	critical splice donor site	probably null
R6219:Lama1	UTSW	17	67,790,856 (GRCm38)	missense	probably benign	0.08
R6224:Lama1	UTSW	17	67,802,987 (GRCm38)	missense	possibly damaging	0.56
R6249:Lama1	UTSW	17	67,798,604 (GRCm38)	missense	probably benign
R6265:Lama1	UTSW	17	67,750,655 (GRCm38)	missense	probably damaging	0.98
R6276:Lama1	UTSW	17	67,784,088 (GRCm38)	splice site	probably null
R6284:Lama1	UTSW	17	67,810,096 (GRCm38)	missense	probably damaging	0.99
R6337:Lama1	UTSW	17	67,786,019 (GRCm38)	missense	probably benign	0.27
R6414:Lama1	UTSW	17	67,746,910 (GRCm38)	critical splice donor site	probably null
R6631:Lama1	UTSW	17	67,774,482 (GRCm38)	missense	probably benign	0.21
R6659:Lama1	UTSW	17	67,818,635 (GRCm38)	missense	probably damaging	1.00
R6660:Lama1	UTSW	17	67,804,500 (GRCm38)	missense	probably benign	0.05
R6677:Lama1	UTSW	17	67,795,233 (GRCm38)	missense	probably benign	0.14
R6763:Lama1	UTSW	17	67,746,873 (GRCm38)	missense	unknown
R6787:Lama1	UTSW	17	67,784,025 (GRCm38)	missense	unknown
R6831:Lama1	UTSW	17	67,756,754 (GRCm38)	missense	possibly damaging	0.89
R6855:Lama1	UTSW	17	67,782,155 (GRCm38)	missense	possibly damaging	0.95
R6910:Lama1	UTSW	17	67,791,464 (GRCm38)	missense	possibly damaging	0.60
R6934:Lama1	UTSW	17	67,774,543 (GRCm38)	missense	probably benign	0.04
R6945:Lama1	UTSW	17	67,813,866 (GRCm38)	missense
R6984:Lama1	UTSW	17	67,779,112 (GRCm38)	missense
R6989:Lama1	UTSW	17	67,753,758 (GRCm38)	missense
R6994:Lama1	UTSW	17	67,753,825 (GRCm38)	missense
R6995:Lama1	UTSW	17	67,753,825 (GRCm38)	missense
R7035:Lama1	UTSW	17	67,781,049 (GRCm38)	missense
R7133:Lama1	UTSW	17	67,782,146 (GRCm38)	missense
R7172:Lama1	UTSW	17	67,804,545 (GRCm38)	missense
R7197:Lama1	UTSW	17	67,737,705 (GRCm38)	nonsense	probably null
R7217:Lama1	UTSW	17	67,764,673 (GRCm38)	missense
R7229:Lama1	UTSW	17	67,752,446 (GRCm38)	missense
R7264:Lama1	UTSW	17	67,743,297 (GRCm38)	missense
R7311:Lama1	UTSW	17	67,767,385 (GRCm38)	missense
R7394:Lama1	UTSW	17	67,717,261 (GRCm38)	missense
R7419:Lama1	UTSW	17	67,717,174 (GRCm38)	missense
R7460:Lama1	UTSW	17	67,767,018 (GRCm38)	missense
R7492:Lama1	UTSW	17	67,817,651 (GRCm38)	missense
R7494:Lama1	UTSW	17	67,811,446 (GRCm38)	missense
R7552:Lama1	UTSW	17	67,737,667 (GRCm38)	missense
R7576:Lama1	UTSW	17	67,782,041 (GRCm38)	missense
R7583:Lama1	UTSW	17	67,761,621 (GRCm38)	missense
R7649:Lama1	UTSW	17	67,737,554 (GRCm38)	missense
R7663:Lama1	UTSW	17	67,780,880 (GRCm38)	missense
R7667:Lama1	UTSW	17	67,780,597 (GRCm38)	missense
R7688:Lama1	UTSW	17	67,761,628 (GRCm38)	missense
R7693:Lama1	UTSW	17	67,817,031 (GRCm38)	missense
R7748:Lama1	UTSW	17	67,750,590 (GRCm38)	missense
R7778:Lama1	UTSW	17	67,804,473 (GRCm38)	missense
R7824:Lama1	UTSW	17	67,804,473 (GRCm38)	missense
R7861:Lama1	UTSW	17	67,809,221 (GRCm38)	missense
R7884:Lama1	UTSW	17	67,769,435 (GRCm38)	missense
R8029:Lama1	UTSW	17	67,817,594 (GRCm38)	missense
R8078:Lama1	UTSW	17	67,791,294 (GRCm38)	missense
R8101:Lama1	UTSW	17	67,745,922 (GRCm38)	missense
R8313:Lama1	UTSW	17	67,750,520 (GRCm38)	missense
R8356:Lama1	UTSW	17	67,737,496 (GRCm38)	missense
R8366:Lama1	UTSW	17	67,818,704 (GRCm38)	missense
R8403:Lama1	UTSW	17	67,745,923 (GRCm38)	missense
R8456:Lama1	UTSW	17	67,737,496 (GRCm38)	missense
R8466:Lama1	UTSW	17	67,813,953 (GRCm38)	missense
R8678:Lama1	UTSW	17	67,817,103 (GRCm38)	missense
R8728:Lama1	UTSW	17	67,818,668 (GRCm38)	missense
R8796:Lama1	UTSW	17	67,810,151 (GRCm38)	missense
R8885:Lama1	UTSW	17	67,773,784 (GRCm38)	missense
R8893:Lama1	UTSW	17	67,805,372 (GRCm38)	missense
R8898:Lama1	UTSW	17	67,821,615 (GRCm38)	missense
R8909:Lama1	UTSW	17	67,772,741 (GRCm38)	missense
R9025:Lama1	UTSW	17	67,812,496 (GRCm38)	missense
R9045:Lama1	UTSW	17	67,753,843 (GRCm38)	missense
R9098:Lama1	UTSW	17	67,804,513 (GRCm38)	missense
R9114:Lama1	UTSW	17	67,821,674 (GRCm38)	missense
R9173:Lama1	UTSW	17	67,769,602 (GRCm38)	missense
R9190:Lama1	UTSW	17	67,804,519 (GRCm38)	missense
R9381:Lama1	UTSW	17	67,737,484 (GRCm38)	missense
R9429:Lama1	UTSW	17	67,811,454 (GRCm38)	missense
R9504:Lama1	UTSW	17	67,821,666 (GRCm38)	missense
R9558:Lama1	UTSW	17	67,817,009 (GRCm38)	missense
R9647:Lama1	UTSW	17	67,717,175 (GRCm38)	missense
R9651:Lama1	UTSW	17	67,794,220 (GRCm38)	missense
R9654:Lama1	UTSW	17	67,794,271 (GRCm38)	missense
R9710:Lama1	UTSW	17	67,822,409 (GRCm38)	missense
R9733:Lama1	UTSW	17	67,809,945 (GRCm38)	missense
RF001:Lama1	UTSW	17	67,752,902 (GRCm38)	missense
RF013:Lama1	UTSW	17	67,781,062 (GRCm38)	missense
V8831:Lama1	UTSW	17	67,752,883 (GRCm38)	missense	probably benign	0.00
X0024:Lama1	UTSW	17	67,738,888 (GRCm38)	missense	probably damaging	1.00
X0028:Lama1	UTSW	17	67,794,310 (GRCm38)	missense	probably benign	0.06
X0028:Lama1	UTSW	17	67,767,422 (GRCm38)	missense	probably benign	0.00
X0066:Lama1	UTSW	17	67,811,566 (GRCm38)	missense	probably damaging	1.00
Z1088:Lama1	UTSW	17	67,810,171 (GRCm38)	missense	probably damaging	1.00
Z1088:Lama1	UTSW	17	67,771,082 (GRCm38)	missense	probably benign	0.25
Z1088:Lama1	UTSW	17	67,752,883 (GRCm38)	missense	probably benign	0.00
Z1176:Lama1	UTSW	17	67,752,883 (GRCm38)	missense	probably benign	0.00
Z1177:Lama1	UTSW	17	67,752,883 (GRCm38)	missense	probably benign	0.00
Z1191:Lama1	UTSW	17	67,798,644 (GRCm38)	missense

Posted On

2014-05-07