ClinVar Miner

List of variants in gene LAMA4 reported as likely benign for not provided

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Total variants: 45
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HGVS dbSNP
NC_000006.12:g.112141152del
NM_001105206.3(LAMA4):c.1077+286C>T
NM_001105206.3(LAMA4):c.1190-132C>T
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr) rs200112094
NM_001105206.3(LAMA4):c.1357+312T>A
NM_001105206.3(LAMA4):c.1551+279G>A
NM_001105206.3(LAMA4):c.1552-184A>G
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1668+155A>T
NM_001105206.3(LAMA4):c.1677A>G (p.Ser559=)
NM_001105206.3(LAMA4):c.1817+111G>A
NM_001105206.3(LAMA4):c.2056+70G>A
NM_001105206.3(LAMA4):c.2057-129A>G
NM_001105206.3(LAMA4):c.2057-210T>C
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2354-114dup
NM_001105206.3(LAMA4):c.2398C>T (p.Arg800Cys) rs202184174
NM_001105206.3(LAMA4):c.2493+125del
NM_001105206.3(LAMA4):c.2493+214A>G
NM_001105206.3(LAMA4):c.2494-115A>G
NM_001105206.3(LAMA4):c.2667+118A>G
NM_001105206.3(LAMA4):c.2668-153A>C
NM_001105206.3(LAMA4):c.2813+70C>T
NM_001105206.3(LAMA4):c.297+260T>C
NM_001105206.3(LAMA4):c.2977-16T>A
NM_001105206.3(LAMA4):c.3110+116A>C
NM_001105206.3(LAMA4):c.3558-14A>C
NM_001105206.3(LAMA4):c.3696+13C>T
NM_001105206.3(LAMA4):c.3969-312T>A
NM_001105206.3(LAMA4):c.4475+114T>C
NM_001105206.3(LAMA4):c.4475+74G>T
NM_001105206.3(LAMA4):c.4821+37T>G
NM_001105206.3(LAMA4):c.4822-192A>G
NM_001105206.3(LAMA4):c.503+49C>A
NM_001105206.3(LAMA4):c.503+71C>G
NM_001105206.3(LAMA4):c.503+88A>C
NM_001105206.3(LAMA4):c.5113-137C>T
NM_001105206.3(LAMA4):c.5327-178T>C
NM_001105206.3(LAMA4):c.5327-301C>A
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.668G>A (p.Arg223His) rs200017155
NM_001105206.3(LAMA4):c.815-13G>C
NM_001105206.3(LAMA4):c.966+308C>T
NM_001105206.3(LAMA4):c.967-228C>A
NM_001105206.3(LAMA4):c.967-57A>G

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