ClinVar Miner

List of variants in gene SUN2 reported as likely benign for hereditary skeletal muscle disorder

Included ClinVar conditions (591):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_015374.3(SUN2):c.467G>A (p.Arg156Gln) rs137925849 0.00125
NM_015374.3(SUN2):c.28C>T (p.Arg10Cys) rs139611023 0.00063
NM_015374.3(SUN2):c.686-12C>T rs372413342 0.00038
NM_015374.3(SUN2):c.432G>A (p.Ser144=) rs140094524 0.00034
NM_015374.3(SUN2):c.657G>A (p.Pro219=) rs143617240 0.00026
NM_015374.3(SUN2):c.615-10C>T rs375410049 0.00024
NM_015374.3(SUN2):c.461G>A (p.Arg154Gln) rs143392390 0.00017
NM_015374.3(SUN2):c.425-11G>A rs774550032 0.00016
NM_015374.3(SUN2):c.615-11G>A rs368890492 0.00016
NM_015374.3(SUN2):c.287-16G>A rs749337613 0.00014
NM_015374.3(SUN2):c.425-9T>C rs375405393 0.00013
NM_015374.3(SUN2):c.635C>T (p.Thr212Met) rs142155226 0.00013
NM_015374.3(SUN2):c.396G>A (p.Ser132=) rs374648086 0.00012
NM_015374.3(SUN2):c.520+8G>A rs201387591 0.00011
NM_015374.3(SUN2):c.672G>A (p.Thr224=) rs767229084 0.00010
NM_015374.3(SUN2):c.425-4G>A rs372875785 0.00009
NM_015374.3(SUN2):c.773A>G (p.Asp258Gly) rs201945306 0.00009
NM_015374.3(SUN2):c.51C>T (p.Asp17=) rs759125687 0.00008
NM_015374.3(SUN2):c.459G>A (p.Ser153=) rs138320872 0.00006
NM_015374.3(SUN2):c.615-9G>A rs757921553 0.00006
NM_015374.3(SUN2):c.45C>T (p.Asp15=) rs146335558 0.00005
NM_015374.3(SUN2):c.726C>T (p.His242=) rs539723941 0.00005
NM_015374.3(SUN2):c.624G>A (p.Ser208=) rs747299144 0.00004
NM_015374.3(SUN2):c.763A>C (p.Arg255=) rs781191176 0.00004
NM_015374.3(SUN2):c.147C>T (p.Asn49=) rs769644853 0.00003
NM_015374.3(SUN2):c.243A>C (p.Pro81=) rs745316329 0.00003
NM_015374.3(SUN2):c.636G>A (p.Thr212=) rs200221237 0.00003
NM_015374.3(SUN2):c.681G>A (p.Thr227=) rs754563807 0.00003
NM_015374.3(SUN2):c.168G>A (p.Ala56=) rs561928372 0.00002
NM_015374.3(SUN2):c.333G>A (p.Glu111=) rs772494839 0.00002
NM_015374.3(SUN2):c.516G>A (p.Ser172=) rs545823498 0.00002
NM_015374.3(SUN2):c.633G>A (p.Lys211=) rs1347064197 0.00002
NM_015374.3(SUN2):c.741C>T (p.Ser247=) rs1342698251 0.00002
NM_015374.3(SUN2):c.231G>A (p.Glu77=) rs760297349 0.00001
NM_015374.3(SUN2):c.342G>A (p.Arg114=) rs773389007 0.00001
NM_015374.3(SUN2):c.357G>A (p.Val119=) rs1603229883 0.00001
NM_015374.3(SUN2):c.425-12C>T rs773495171 0.00001
NM_015374.3(SUN2):c.474C>T (p.Ala158=) rs1211809169 0.00001
NM_015374.3(SUN2):c.57C>T (p.Ser19=) rs374169188 0.00001
NM_015374.3(SUN2):c.603C>T (p.Phe201=) rs1048872109 0.00001
NM_015374.3(SUN2):c.122+17G>A
NM_015374.3(SUN2):c.123-14T>C rs759683752
NM_015374.3(SUN2):c.123-19C>G rs767573606
NM_015374.3(SUN2):c.126C>A (p.Thr42=)
NM_015374.3(SUN2):c.165A>C (p.Pro55=)
NM_015374.3(SUN2):c.183G>A (p.Pro61=)
NM_015374.3(SUN2):c.247A>C (p.Arg83=) rs1474913633
NM_015374.3(SUN2):c.252C>T (p.Ser84=)
NM_015374.3(SUN2):c.255C>G (p.Ser85=)
NM_015374.3(SUN2):c.261G>A (p.Glu87=)
NM_015374.3(SUN2):c.286+12G>T rs2146081428
NM_015374.3(SUN2):c.286+19G>A
NM_015374.3(SUN2):c.287-17G>C
NM_015374.3(SUN2):c.287-7T>C rs1603230014
NM_015374.3(SUN2):c.306G>A (p.Arg102=)
NM_015374.3(SUN2):c.321G>A (p.Thr107=)
NM_015374.3(SUN2):c.348C>T (p.Ser116=)
NM_015374.3(SUN2):c.405C>T (p.Ser135=)
NM_015374.3(SUN2):c.425-4G>T
NM_015374.3(SUN2):c.450T>C (p.Ser150=)
NM_015374.3(SUN2):c.486G>A (p.Ala162=)
NM_015374.3(SUN2):c.520+14C>T
NM_015374.3(SUN2):c.520+18C>G
NM_015374.3(SUN2):c.521-20C>T
NM_015374.3(SUN2):c.561C>G (p.Thr187=) rs775025047
NM_015374.3(SUN2):c.567C>T (p.Tyr189=)
NM_015374.3(SUN2):c.614+14C>T
NM_015374.3(SUN2):c.614+18C>T
NM_015374.3(SUN2):c.615-12C>T
NM_015374.3(SUN2):c.628C>T (p.Leu210=)
NM_015374.3(SUN2):c.66C>T (p.Ser22=)
NM_015374.3(SUN2):c.686-13C>G
NM_015374.3(SUN2):c.686-13C>T
NM_015374.3(SUN2):c.705C>T (p.Pro235=)
NM_015374.3(SUN2):c.753G>A (p.Ala251=)
NM_015374.3(SUN2):c.771G>A (p.Pro257=)
NM_015374.3(SUN2):c.78G>A (p.Ser26=) rs757655044
NM_015374.3(SUN2):c.78G>T (p.Ser26=)
NM_015374.3(SUN2):c.801G>A (p.Ser267=)

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