ClinVar Miner

List of variants in gene LAMA2 reported by Counsyl

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 172
Download table as spreadsheet
HGVS dbSNP
NM_000426.3(LAMA2):c.1027+1G>T rs1064797327
NM_000426.3(LAMA2):c.106C>T (p.Gln36Ter) rs1360796756
NM_000426.3(LAMA2):c.112+1G>A rs398123367
NM_000426.3(LAMA2):c.1122del (p.Gly376fs) rs1338860420
NM_000426.3(LAMA2):c.1303C>T (p.Arg435Ter) rs773209126
NM_000426.3(LAMA2):c.1306+2T>G rs1326401124
NM_000426.3(LAMA2):c.1307-1G>A rs1554234051
NM_000426.3(LAMA2):c.1358G>C (p.Cys453Ser) rs1554234086
NM_000426.3(LAMA2):c.1364G>A (p.Arg455Gln) rs201177178
NM_000426.3(LAMA2):c.1415_1429del (p.Ser472_Ser476del) rs1554234118
NM_000426.3(LAMA2):c.1467+2T>C rs1554234163
NM_000426.3(LAMA2):c.1669_1671CAG[1] (p.Gln558del) rs775570308
NM_000426.3(LAMA2):c.1782+2dup rs1272011145
NM_000426.3(LAMA2):c.1793_1795del (p.Val598del) rs1165542235
NM_000426.3(LAMA2):c.1795_1797GGA[1] (p.Gly600del) rs753417521
NM_000426.3(LAMA2):c.2037G>C (p.Ala679=) rs398123369
NM_000426.3(LAMA2):c.2089A>G (p.Ile697Val) rs778059153
NM_000426.3(LAMA2):c.2096+1G>A rs1554256965
NM_000426.3(LAMA2):c.2176T>C (p.Cys726Arg) rs920771326
NM_000426.3(LAMA2):c.21_23CCT[4] (p.Leu13dup) rs1347823295
NM_000426.3(LAMA2):c.2217G>T (p.Trp739Cys) rs192317605
NM_000426.3(LAMA2):c.2230C>T (p.Arg744Ter) rs775676341
NM_000426.3(LAMA2):c.2322+1G>C rs945091158
NM_000426.3(LAMA2):c.2323-1G>A rs1278823424
NM_000426.3(LAMA2):c.2375T>C (p.Phe792Ser) rs398123370
NM_000426.3(LAMA2):c.2450+5_2450+8delGTAA rs1554260313
NM_000426.3(LAMA2):c.2451-1delG rs767784355
NM_000426.3(LAMA2):c.2451-2A>G rs993196576
NM_000426.3(LAMA2):c.2451-6A>G rs896691971
NM_000426.3(LAMA2):c.2461A>C (p.Thr821Pro) rs186538779
NM_000426.3(LAMA2):c.2462C>T (p.Thr821Met) rs117422805
NM_000426.3(LAMA2):c.2749+1G>A rs759555791
NM_000426.3(LAMA2):c.2749+1G>C rs759555791
NM_000426.3(LAMA2):c.2749+2dup rs759144210
NM_000426.3(LAMA2):c.283+1G>A rs200288072
NM_000426.3(LAMA2):c.283C>T (p.Gln95Ter) rs1018100729
NM_000426.3(LAMA2):c.2962C>T (p.Gln988Ter) rs398123371
NM_000426.3(LAMA2):c.2T>C (p.Met1Thr) rs374403765
NM_000426.3(LAMA2):c.3085C>T (p.Arg1029Ter) rs145420388
NM_000426.3(LAMA2):c.30_32del (p.Leu13del) rs1278217420
NM_000426.3(LAMA2):c.3110T>C (p.Ile1037Thr) rs797045679
NM_000426.3(LAMA2):c.3279C>T (p.Cys1093=) rs371376404
NM_000426.3(LAMA2):c.3283C>T (p.Arg1095Ter) rs376088608
NM_000426.3(LAMA2):c.3294del (p.His1097_Trp1098insTer) rs764839142
NM_000426.3(LAMA2):c.329G>A (p.Trp110Ter) rs1441933780
NM_000426.3(LAMA2):c.3556-13T>A rs775278003
NM_000426.3(LAMA2):c.3623_3645del (p.Lys1208fs) rs727503992
NM_000426.3(LAMA2):c.363C>A (p.Tyr121Ter) rs535635043
NM_000426.3(LAMA2):c.3718C>T (p.Gln1240Ter) rs121913569
NM_000426.3(LAMA2):c.3736-2A>G rs372715292
NM_000426.3(LAMA2):c.3736-2A>T rs372715292
NM_000426.3(LAMA2):c.3799_3821del (p.Phe1267fs) rs750220830
NM_000426.3(LAMA2):c.3861C>T (p.Ile1287=) rs138702650
NM_000426.3(LAMA2):c.396+1G>T rs770617208
NM_000426.3(LAMA2):c.3976C>T (p.Arg1326Ter) rs398123373
NM_000426.3(LAMA2):c.4010A>G (p.His1337Arg) rs139739075
NM_000426.3(LAMA2):c.4019_4024dup (p.Lys1342_Ala1343insIleIle) rs1554270059
NM_000426.3(LAMA2):c.4048C>T (p.Arg1350Ter) rs756854513
NM_000426.3(LAMA2):c.4107_4109del (p.Met1370del) rs1446213044
NM_000426.3(LAMA2):c.4176+1G>A rs1404492484
NM_000426.3(LAMA2):c.4198C>T (p.Arg1400Ter) rs775112258
NM_000426.3(LAMA2):c.4232G>A (p.Gly1411Glu) rs727502850
NM_000426.3(LAMA2):c.4348C>T (p.Arg1450Ter) rs200923373
NM_000426.3(LAMA2):c.437C>T (p.Ser146Phe) rs143680577
NM_000426.3(LAMA2):c.4436+1G>C rs376430565
NM_000426.3(LAMA2):c.4468_4470GAC[1] (p.Asp1491del) rs1554277753
NM_000426.3(LAMA2):c.4477C>T (p.Arg1493Cys) rs751053800
NM_000426.3(LAMA2):c.4517G>C (p.Cys1506Ser) rs1409043489
NM_000426.3(LAMA2):c.4524-2A>T rs1554278541
NM_000426.3(LAMA2):c.4640C>T (p.Thr1547Met) rs778106503
NM_000426.3(LAMA2):c.4645C>T (p.Arg1549Ter) rs121913575
NM_000426.3(LAMA2):c.4660_4668del (p.Gly1554_Lys1556del) rs1554278670
NM_000426.3(LAMA2):c.4692_4695dup (p.Arg1566fs) rs774051471
NM_000426.3(LAMA2):c.4717+1G>C rs1131691660
NM_000426.3(LAMA2):c.4717+1G>T rs1131691660
NM_000426.3(LAMA2):c.4743_4745TCT[1] (p.Leu1583del) rs1554281282
NM_000426.3(LAMA2):c.476_478ATG[1] (p.Asp160del) rs1192484658
NM_000426.3(LAMA2):c.498G>A (p.Trp166Ter) rs553221833
NM_000426.3(LAMA2):c.5050G>T (p.Glu1684Ter) rs201632009
NM_000426.3(LAMA2):c.5072-3C>A rs759155854
NM_000426.3(LAMA2):c.5116C>T (p.Arg1706Ter) rs758775001
NM_000426.3(LAMA2):c.5156_5159del (p.Lys1719fs) rs1554286963
NM_000426.3(LAMA2):c.5169_5171GAT[1] (p.Met1724del) rs1554286976
NM_000426.3(LAMA2):c.5235-18G>A rs188365084
NM_000426.3(LAMA2):c.5259del (p.Lys1753_Val1754insTer) rs1211739649
NM_000426.3(LAMA2):c.5260del (p.Lys1753_Val1754insTer) rs794727594
NM_000426.3(LAMA2):c.5325dup (p.Leu1776fs) rs768458445
NM_000426.3(LAMA2):c.5449_5451AAG[1] (p.Lys1818del) rs1225610123
NM_000426.3(LAMA2):c.5476C>T (p.Arg1826Ter) rs747349942
NM_000426.3(LAMA2):c.5562+1G>A rs376014152
NM_000426.3(LAMA2):c.5562+5G>C rs771046502
NM_000426.3(LAMA2):c.5665_5667del (p.Lys1889del) rs767066183
NM_000426.3(LAMA2):c.5706_5712del (p.Asp1902fs) rs398123377
NM_000426.3(LAMA2):c.5865+2T>G rs1554290316
NM_000426.3(LAMA2):c.5866-1G>A rs1064797040
NM_000426.3(LAMA2):c.5866-2A>G rs1554295204
NM_000426.3(LAMA2):c.5914C>T (p.Gln1972Ter) rs398123378
NM_000426.3(LAMA2):c.5954_5962dup (p.Ala1985_Asp1987dup) rs1554295259
NM_000426.3(LAMA2):c.595T>A (p.Cys199Ser) rs886043693
NM_000426.3(LAMA2):c.611C>A (p.Ser204Tyr) rs1204310516
NM_000426.3(LAMA2):c.6195_6197GAA[2] (p.Lys2067del) rs758495000
NM_000426.3(LAMA2):c.61C>T (p.Gln21Ter) rs886061039
NM_000426.3(LAMA2):c.6269-820A>G rs544696321
NM_000426.3(LAMA2):c.6269-829A>G rs758519410
NM_000426.3(LAMA2):c.6269-831C>G rs371162111
NM_000426.3(LAMA2):c.6269-831C>T rs371162111
NM_000426.3(LAMA2):c.6269-845C>T rs1554297888
NM_000426.3(LAMA2):c.6269-848T>A rs1554297884
NM_000426.3(LAMA2):c.6269-848T>C rs1554297884
NM_000426.3(LAMA2):c.6269-849C>T rs1554297881
NM_000426.3(LAMA2):c.6269-852A>C rs766496312
NM_000426.3(LAMA2):c.6269-855A>C rs1554297879
NM_000426.3(LAMA2):c.6269-855A>G rs1554297879
NM_000426.3(LAMA2):c.6269-855A>T rs1554297879
NM_000426.3(LAMA2):c.6269-856C>G rs763589558
NM_000426.3(LAMA2):c.6322C>T (p.Arg2108Trp) rs139824017
NM_000426.3(LAMA2):c.640-1G>A rs1296761337
NM_000426.3(LAMA2):c.6429+1G>C rs1262029350
NM_000426.3(LAMA2):c.6429+1G>T rs1262029350
NM_000426.3(LAMA2):c.6510_6512TGT[1] (p.Val2172del) rs1363017615
NM_000426.3(LAMA2):c.6563G>A (p.Ser2188Asn) rs372592018
NM_000426.3(LAMA2):c.6573+1G>A rs757435241
NM_000426.3(LAMA2):c.6573+1G>T rs757435241
NM_000426.3(LAMA2):c.6702A>T (p.Ala2234=) rs372212378
NM_000426.3(LAMA2):c.6786G>A (p.Ser2262=) rs398123382
NM_000426.3(LAMA2):c.6919_6920del (p.Tyr2307fs) rs757404275
NM_000426.3(LAMA2):c.6955C>T (p.Arg2319Ter) rs398123383
NM_000426.3(LAMA2):c.6992+5G>A rs1221715098
NM_000426.3(LAMA2):c.6993-2A>C rs200669208
NM_000426.3(LAMA2):c.7074C>A (p.Tyr2358Ter) rs762806915
NM_000426.3(LAMA2):c.7147C>T (p.Arg2383Ter) rs121913576
NM_000426.3(LAMA2):c.715C>T (p.Arg239Cys) rs145465528
NM_000426.3(LAMA2):c.7250A>G (p.His2417Arg) rs147185142
NM_000426.3(LAMA2):c.7286_7288del (p.Arg2429del) rs1350705904
NM_000426.3(LAMA2):c.7369A>C (p.Asn2457His) rs797045680
NM_000426.3(LAMA2):c.7444A>T (p.Lys2482Ter) rs1554303937
NM_000426.3(LAMA2):c.7473A>G (p.Lys2491=) rs886038295
NM_000426.3(LAMA2):c.7490_7493dup (p.Asp2498fs) rs1480934961
NM_000426.3(LAMA2):c.7572+1G>A rs1554305006
NM_000426.3(LAMA2):c.7658del (p.Ser2553fs) rs1293303410
NM_000426.3(LAMA2):c.7732C>T (p.Arg2578Ter) rs121913572
NM_000426.3(LAMA2):c.77_79AGC[4] (p.Gln28dup) rs1554312698
NM_000426.3(LAMA2):c.77_79AGC[5] (p.Gln27_Gln28dup) rs1554312698
NM_000426.3(LAMA2):c.7881T>G (p.His2627Gln) rs202247792
NM_000426.3(LAMA2):c.7888C>T (p.Arg2630Ter) rs727502851
NM_000426.3(LAMA2):c.7933_7941del (p.Tyr2645_Gln2647del) rs762065775
NM_000426.3(LAMA2):c.8076-1G>A rs1554310169
NM_000426.3(LAMA2):c.8169_8173del (p.Ala2723_Pro2724insTer) rs1554310242
NM_000426.3(LAMA2):c.817A>T (p.Arg273Ter) rs886043648
NM_000426.3(LAMA2):c.819+1G>A rs1554226186
NM_000426.3(LAMA2):c.819+2dup rs765817742
NM_000426.3(LAMA2):c.8244+1G>A rs749522728
NM_000426.3(LAMA2):c.830C>T (p.Ser277Leu) rs398123388
NM_000426.3(LAMA2):c.8326A>T (p.Ile2776Phe) rs569286697
NM_000426.3(LAMA2):c.8548-2A>G rs369224209
NM_000426.3(LAMA2):c.8654T>C (p.Leu2885Pro) rs1554316199
NM_000426.3(LAMA2):c.8710_8712dup (p.Tyr2904dup) rs1554317110
NM_000426.3(LAMA2):c.8716_8717insCCA (p.Ile2906_Asp2907insThr) rs1554317120
NM_000426.3(LAMA2):c.8768_8770AAC[1] (p.Gln2924del) rs1554317173
NM_000426.3(LAMA2):c.8836G>A (p.Gly2946Arg) rs370843758
NM_000426.3(LAMA2):c.8858-1G>A rs1554319117
NM_000426.3(LAMA2):c.8907C>T (p.Arg2969=) rs367622610
NM_000426.3(LAMA2):c.8989-12C>G rs144860334
NM_000426.3(LAMA2):c.8992_8994dup (p.Met2998dup) rs1437850233
NM_000426.3(LAMA2):c.9095dup (p.Ile3033fs) rs1554320205
NM_000426.3(LAMA2):c.9145C>G (p.Gln3049Glu) rs146525742
NM_000426.3(LAMA2):c.9211+1G>A rs1554320318
NM_000426.3(LAMA2):c.9211+6T>C rs201375881
NM_000426.3(LAMA2):c.9212-2A>G rs1554321125
NM_000426.3(LAMA2):c.9266_9283dup (p.Arg3089_Thr3094dup) rs1554321180
NM_000426.3(LAMA2):c.9295A>T (p.Lys3099Ter) rs749797580
NM_000426.3(LAMA2):c.951_952insCT (p.Cys318fs) rs1554227092

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.