ClinVar Miner

List of variants in gene SYNE1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_182961.4(SYNE1):c.25856T>C (p.Leu8619Pro) rs139834542 0.00178
NM_182961.4(SYNE1):c.4107T>A (p.Phe1369Leu) rs149109801 0.00172
NM_182961.4(SYNE1):c.20288C>T (p.Ser6763Leu) rs115534729 0.00137
NM_182961.4(SYNE1):c.4822G>A (p.Ala1608Thr) rs138617999 0.00106
NM_182961.4(SYNE1):c.17827T>C (p.Ser5943Pro) rs147998933 0.00101
NM_182961.4(SYNE1):c.14263C>T (p.Leu4755Phe) rs41301343 0.00100
NM_182961.4(SYNE1):c.5125C>A (p.Gln1709Lys) rs140005424 0.00052
NM_182961.4(SYNE1):c.23260G>A (p.Val7754Ile) rs150550013 0.00042
NM_182961.4(SYNE1):c.19635G>T (p.Arg6545Ser) rs147143947 0.00032
NM_182961.4(SYNE1):c.7435A>G (p.Lys2479Glu) rs188146577 0.00027
NM_182961.4(SYNE1):c.22346+6G>T rs368678916 0.00020
NM_182961.4(SYNE1):c.15863G>C (p.Gly5288Ala) rs201313856 0.00018
NM_182961.4(SYNE1):c.7076C>A (p.Thr2359Asn) rs142747430 0.00014
NM_182961.4(SYNE1):c.18584A>C (p.Gln6195Pro) rs370472085 0.00011
NM_182961.4(SYNE1):c.22303C>T (p.Arg7435Cys) rs371642308 0.00011
NM_182961.4(SYNE1):c.10217A>C (p.Asp3406Ala) rs546645393 0.00010
NM_182961.4(SYNE1):c.1708T>C (p.Tyr570His) rs199962439 0.00009
NM_182961.4(SYNE1):c.3433A>G (p.Thr1145Ala) rs148733093 0.00006
NM_182961.4(SYNE1):c.5049G>T (p.Met1683Ile) rs755866233 0.00006
NM_182961.4(SYNE1):c.18727G>A (p.Glu6243Lys) rs200360218 0.00005
NM_182961.4(SYNE1):c.20449C>T (p.Arg6817Trp) rs140903556 0.00004
NM_182961.4(SYNE1):c.7592T>C (p.Ile2531Thr) rs138766629 0.00004
NM_182961.4(SYNE1):c.12388C>G (p.Gln4130Glu) rs779969031 0.00003
NM_182961.4(SYNE1):c.13922T>A (p.Leu4641His) rs199673397 0.00003
NM_182961.4(SYNE1):c.18622C>G (p.Gln6208Glu) rs558425673 0.00003
NM_182961.4(SYNE1):c.18631G>A (p.Gly6211Ser) rs149624155 0.00003
NM_182961.4(SYNE1):c.14533C>T (p.His4845Tyr) rs373200852 0.00001
NM_182961.4(SYNE1):c.15124G>C (p.Glu5042Gln) rs533927341 0.00001
NM_182961.4(SYNE1):c.20613G>T (p.Lys6871Asn) rs767727011 0.00001
NM_182961.4(SYNE1):c.23243C>G (p.Ser7748Cys) rs1289070478 0.00001
NM_182961.4(SYNE1):c.12466A>G (p.Met4156Val)
NM_182961.4(SYNE1):c.1484C>T (p.Thr495Ile) rs2154279162
NM_182961.4(SYNE1):c.17639G>T (p.Arg5880Leu) rs767844376
NM_182961.4(SYNE1):c.22873G>A (p.Val7625Met) rs749743156
NM_182961.4(SYNE1):c.3977G>A (p.Arg1326His) rs371842938
NM_182961.4(SYNE1):c.4946C>T (p.Ala1649Val)

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