ClinVar Miner

List of variants in gene LAMA3 reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_198129.4(LAMA3):c.8708+1G>A rs754558574 0.00003
NM_198129.4(LAMA3):c.4999-1G>A rs1327684674 0.00001
NM_198129.4(LAMA3):c.4999-2A>C rs761269065 0.00001
NM_198129.4(LAMA3):c.5113-2A>G rs1057516475 0.00001
NM_198129.4(LAMA3):c.7158+1G>A rs1057516279 0.00001
NM_198129.4(LAMA3):c.8295+2T>C rs1555743457 0.00001
NM_198129.4(LAMA3):c.9642+1G>A rs780861460 0.00001
NC_000018.9:g.(?_21473162)_(21481161_?)del
NM_198129.4(LAMA3):c.5061C>A (p.Cys1687Ter) rs2144862529
NM_198129.4(LAMA3):c.5112+1G>A rs1057517023
NM_198129.4(LAMA3):c.5112+1G>T rs1057517023
NM_198129.4(LAMA3):c.5223-2A>G
NM_198129.4(LAMA3):c.5410_5410+1delinsAT rs2145011788
NM_198129.4(LAMA3):c.5411-2_5411-1delinsGA rs1555728297
NM_198129.4(LAMA3):c.5461+1G>A rs1555728319
NM_198129.4(LAMA3):c.5461+2T>G rs2145055524
NM_198129.4(LAMA3):c.5462-1G>A
NM_198129.4(LAMA3):c.5613+2T>C
NM_198129.4(LAMA3):c.5614-2A>G
NM_198129.4(LAMA3):c.5633del (p.Arg1878fs)
NM_198129.4(LAMA3):c.5724+2T>C
NM_198129.4(LAMA3):c.5725-1G>A
NM_198129.4(LAMA3):c.5837-2A>G
NM_198129.4(LAMA3):c.6004+2T>C rs2080993755
NM_198129.4(LAMA3):c.6201+1G>C
NM_198129.4(LAMA3):c.6202-2A>T
NM_198129.4(LAMA3):c.6299del (p.Leu2100fs)
NM_198129.4(LAMA3):c.6473+2T>A
NM_198129.4(LAMA3):c.6719-2A>T
NM_198129.4(LAMA3):c.6836-1G>A
NM_198129.4(LAMA3):c.7016-1G>A
NM_198129.4(LAMA3):c.7159-1G>T
NM_198129.4(LAMA3):c.7329+1G>A
NM_198129.4(LAMA3):c.7459A>T (p.Met2487Leu) rs1085308017
NM_198129.4(LAMA3):c.7461_7481+17del rs1555737629
NM_198129.4(LAMA3):c.7481+1G>T rs1599082889
NM_198129.4(LAMA3):c.7778+1G>A rs2145252486
NM_198129.4(LAMA3):c.7923+2T>C
NM_198129.4(LAMA3):c.8177+2T>G rs786204732
NM_198129.4(LAMA3):c.8308G>C (p.Ala2770Pro) rs1131691680
NM_198129.4(LAMA3):c.8863-1G>A
NM_198129.4(LAMA3):c.9027-1G>A
NM_198129.4(LAMA3):c.9027-2A>G
NM_198129.4(LAMA3):c.9210+2T>G rs940016371
NM_198129.4(LAMA3):c.9352-2A>G rs2082838403
NM_198129.4(LAMA3):c.9512-2A>G

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.