ClinVar Miner

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

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Gene type:
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Total variants: 79
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HGVS dbSNP
GRCh37/hg19 6q21(chr6:112512882-112633545)x3
GRCh37/hg19 6q21(chr6:112531660-112612615)x3
NC_000006.12:g.112150420_112150423del
NC_000006.12:g.112154657del
NC_000006.12:g.112158541_112158544del
NC_000006.12:g.112159133del
NM_001105206.3(LAMA4):c.1077+64C>T
NM_001105206.3(LAMA4):c.1078-195T>A
NM_001105206.3(LAMA4):c.1078-201A>T
NM_001105206.3(LAMA4):c.1078-222C>A
NM_001105206.3(LAMA4):c.1189+78C>T
NM_001105206.3(LAMA4):c.1190-165C>T
NM_001105206.3(LAMA4):c.1669-286_1669-285del
NM_001105206.3(LAMA4):c.1817+42G>A
NM_001105206.3(LAMA4):c.1818-231C>G
NM_001105206.3(LAMA4):c.196-191T>C
NM_001105206.3(LAMA4):c.196-304A>G
NM_001105206.3(LAMA4):c.1960-61A>G
NM_001105206.3(LAMA4):c.2056+196G>A
NM_001105206.3(LAMA4):c.2056+40G>T
NM_001105206.3(LAMA4):c.2057-176T>C
NM_001105206.3(LAMA4):c.2173+251C>G
NM_001105206.3(LAMA4):c.2173+25C>G
NM_001105206.3(LAMA4):c.2174-180A>T
NM_001105206.3(LAMA4):c.2174-28A>C
NM_001105206.3(LAMA4):c.2353+180A>G
NM_001105206.3(LAMA4):c.2354-323A>G
NM_001105206.3(LAMA4):c.2494-199C>T
NM_001105206.3(LAMA4):c.2494-209dup
NM_001105206.3(LAMA4):c.2667+245A>G
NM_001105206.3(LAMA4):c.2668-177C>T
NM_001105206.3(LAMA4):c.297+72T>C
NM_001105206.3(LAMA4):c.298-104T>C
NM_001105206.3(LAMA4):c.298-135T>C
NM_001105206.3(LAMA4):c.298-179C>A
NM_001105206.3(LAMA4):c.298-213A>T
NM_001105206.3(LAMA4):c.298-247T>G
NM_001105206.3(LAMA4):c.298-267T>C
NM_001105206.3(LAMA4):c.3111-155C>T
NM_001105206.3(LAMA4):c.3111-48C>T
NM_001105206.3(LAMA4):c.3414+169A>G
NM_001105206.3(LAMA4):c.3414+180T>A
NM_001105206.3(LAMA4):c.3415-316_3415-313del
NM_001105206.3(LAMA4):c.3696+109C>T
NM_001105206.3(LAMA4):c.3835-258C>T
NM_001105206.3(LAMA4):c.4134-243A>G
NM_001105206.3(LAMA4):c.4134-74C>G
NM_001105206.3(LAMA4):c.422+210G>C
NM_001105206.3(LAMA4):c.422+312C>T
NM_001105206.3(LAMA4):c.422+313A>G
NM_001105206.3(LAMA4):c.423-202C>T
NM_001105206.3(LAMA4):c.4287+211G>A
NM_001105206.3(LAMA4):c.4475+125C>T
NM_001105206.3(LAMA4):c.4475+83C>T
NM_001105206.3(LAMA4):c.4476-153T>C
NM_001105206.3(LAMA4):c.4476-80del
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser) rs12110554
NM_001105206.3(LAMA4):c.4666-277G>A
NM_001105206.3(LAMA4):c.4821+160C>A
NM_001105206.3(LAMA4):c.4821+219C>G
NM_001105206.3(LAMA4):c.4821+245A>G
NM_001105206.3(LAMA4):c.4822-156G>C
NM_001105206.3(LAMA4):c.4981+29del
NM_001105206.3(LAMA4):c.503+93G>T
NM_001105206.3(LAMA4):c.5112+245C>T
NM_001105206.3(LAMA4):c.5113-111_5113-110del
NM_001105206.3(LAMA4):c.5113-166G>A
NM_001105206.3(LAMA4):c.5113-239C>A
NM_001105206.3(LAMA4):c.5206+184C>T
NM_001105206.3(LAMA4):c.5206+59C>A
NM_001105206.3(LAMA4):c.5206+70C>G
NM_001105206.3(LAMA4):c.5207-49_5207-47dup
NM_001105206.3(LAMA4):c.5327-101A>G
NM_001105206.3(LAMA4):c.815-36T>C
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603
NM_001105206.3(LAMA4):c.966+135A>G
NM_001105206.3(LAMA4):c.966+144A>T
NM_001105206.3(LAMA4):c.966+78C>G
NM_001105206.3(LAMA4):c.967-34C>A

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