ClinVar Miner

List of variants in gene LAMA3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_198129.4(LAMA3):c.9211-21C>T rs2288592 0.51885
NM_198129.4(LAMA3):c.5012G>T (p.Gly1671Val) rs142097786 0.00351
NM_198129.4(LAMA3):c.8028C>T (p.Asn2676=) rs35737354 0.00238
NM_198129.4(LAMA3):c.9574A>T (p.Thr3192Ser) rs115991457 0.00234
NM_198129.4(LAMA3):c.8829G>A (p.Arg2943=) rs141472847 0.00103
NM_198129.4(LAMA3):c.2809C>T (p.Leu937Phe) rs61751701 0.00097
NM_198129.4(LAMA3):c.6394T>G (p.Ser2132Ala) rs34590975 0.00063
NM_198129.4(LAMA3):c.2919T>C (p.Asp973=) rs376633949 0.00051
NM_198129.4(LAMA3):c.8069A>G (p.Gln2690Arg) rs147208526 0.00042
NM_198129.4(LAMA3):c.4557C>T (p.Val1519=) rs202215313 0.00040
NM_198129.4(LAMA3):c.8283G>A (p.Ser2761=) rs146634036 0.00039
NM_198129.4(LAMA3):c.7740A>G (p.Thr2580=) rs145848988 0.00033
NM_198129.4(LAMA3):c.1571G>A (p.Arg524His) rs201845068 0.00031
NM_198129.4(LAMA3):c.2374G>A (p.Val792Ile) rs200330511 0.00026
NM_198129.4(LAMA3):c.7310T>C (p.Met2437Thr) rs150804730 0.00021
NM_198129.4(LAMA3):c.8676T>C (p.Phe2892=) rs764132545 0.00021
NM_198129.4(LAMA3):c.1077C>T (p.His359=) rs371273390 0.00019
NM_198129.4(LAMA3):c.4500C>T (p.Asn1500=) rs12607747 0.00017
NM_198129.4(LAMA3):c.6389C>T (p.Ser2130Phe) rs199684626 0.00012
NM_198129.4(LAMA3):c.2937C>T (p.Ser979=) rs148470606 0.00011
NM_198129.4(LAMA3):c.1035C>T (p.Ala345=) rs200144011 0.00009
NM_198129.4(LAMA3):c.4999-9G>A rs774043001 0.00004
NM_198129.4(LAMA3):c.6486C>T (p.Asn2162=) rs185563091 0.00004
NM_198129.4(LAMA3):c.7727A>G (p.Asn2576Ser) rs781529313 0.00001
NM_198129.4(LAMA3):c.9522A>G (p.Val3174=) rs752284879 0.00001
NM_198129.4(LAMA3):c.120G>A (p.Gly40=)
NM_198129.4(LAMA3):c.1273+143C>T
NM_198129.4(LAMA3):c.1273+51C>T
NM_198129.4(LAMA3):c.1350C>T (p.His450=)
NM_198129.4(LAMA3):c.1468+5G>A
NM_198129.4(LAMA3):c.160C>T (p.Leu54=)
NM_198129.4(LAMA3):c.1742-7T>A
NM_198129.4(LAMA3):c.1860G>A (p.Leu620=)
NM_198129.4(LAMA3):c.5133G>A (p.Ala1711=)
NM_198129.4(LAMA3):c.609T>A (p.Asn203Lys)
NM_198129.4(LAMA3):c.7159-10del rs779216497
NM_198129.4(LAMA3):c.7928G>T (p.Arg2643Leu) rs45516998
NM_198129.4(LAMA3):c.8708+4G>A rs200417639

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