ClinVar Miner

List of variants in gene SYNE2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_182914.3(SYNE2):c.17561T>C (p.Leu5854Pro) rs117070973 0.00528
NM_182914.3(SYNE2):c.7162G>A (p.Glu2388Lys) rs200842904 0.00462
NM_182914.3(SYNE2):c.18632C>T (p.Thr6211Met) rs36215895 0.00411
NM_182914.3(SYNE2):c.20011G>A (p.Ala6671Thr) rs34820571 0.00341
NM_182914.3(SYNE2):c.20158C>T (p.Arg6720Trp) rs35700578 0.00335
NM_182914.3(SYNE2):c.11379T>C (p.Leu3793=) rs149391344 0.00319
NM_182914.3(SYNE2):c.4521A>G (p.Gln1507=) rs187183308 0.00204
NM_182914.3(SYNE2):c.20197G>A (p.Glu6733Lys) rs150172232 0.00181
NM_182914.3(SYNE2):c.9230C>T (p.Pro3077Leu) rs200742016 0.00172
NM_182914.3(SYNE2):c.15928T>C (p.Leu5310=) rs74975380 0.00139
NM_182914.3(SYNE2):c.19135C>T (p.Arg6379Cys) rs141741640 0.00138
NM_182914.3(SYNE2):c.3235A>G (p.Thr1079Ala) rs192128801 0.00103
NM_182914.3(SYNE2):c.1873C>T (p.His625Tyr) rs192061494 0.00096
NM_182914.3(SYNE2):c.20161G>A (p.Ala6721Thr) rs140897155 0.00091
NM_182914.3(SYNE2):c.15248A>G (p.Asp5083Gly) rs149617373 0.00086
NM_182914.3(SYNE2):c.3990G>A (p.Ala1330=) rs374980509 0.00064
NM_182914.3(SYNE2):c.4912T>C (p.Tyr1638His) rs146801942 0.00052
NM_182914.3(SYNE2):c.6071C>T (p.Thr2024Ile) rs201401811 0.00046
NM_182914.3(SYNE2):c.14528T>A (p.Phe4843Tyr) rs141488398 0.00042
NM_182914.3(SYNE2):c.9231G>A (p.Pro3077=) rs199659722 0.00041
NM_182914.3(SYNE2):c.13156C>G (p.Gln4386Glu) rs140277551 0.00036
NM_182914.3(SYNE2):c.13570G>A (p.Glu4524Lys) rs143646847 0.00031
NM_182914.3(SYNE2):c.4910A>G (p.Tyr1637Cys) rs143578863 0.00031
NM_182914.3(SYNE2):c.1243G>T (p.Asp415Tyr) rs200836164 0.00027
NM_182914.3(SYNE2):c.20424G>A (p.Ser6808=) rs187841473 0.00027
NM_182914.3(SYNE2):c.10218G>T (p.Leu3406Phe) rs201421128 0.00026
NM_182914.3(SYNE2):c.10815A>T (p.Ser3605=) rs377396543 0.00021
NM_182914.3(SYNE2):c.12903C>T (p.Gly4301=) rs148708516 0.00021
NM_182914.3(SYNE2):c.12655G>A (p.Ala4219Thr) rs138644399 0.00017
NM_182914.3(SYNE2):c.14139+5G>A rs374778697 0.00017
NM_182914.3(SYNE2):c.11061A>G (p.Ala3687=) rs769752720 0.00016
NM_182914.3(SYNE2):c.8911C>G (p.Gln2971Glu) rs200909650 0.00014
NM_182914.3(SYNE2):c.6772G>A (p.Val2258Ile) rs200336916 0.00011
NM_182914.3(SYNE2):c.12379G>A (p.Asp4127Asn) rs145874555 0.00010
NM_182914.3(SYNE2):c.1359T>C (p.Asn453=) rs377273531 0.00010
NM_182914.3(SYNE2):c.5020T>C (p.Leu1674=) rs201666704 0.00010
NM_182914.3(SYNE2):c.19623C>T (p.Asp6541=) rs150366060 0.00009
NM_182914.3(SYNE2):c.16905+4A>C rs369093036 0.00008
NM_182914.3(SYNE2):c.16912G>A (p.Glu5638Lys) rs751734028 0.00008
NM_182914.3(SYNE2):c.14486G>A (p.Cys4829Tyr) rs200997641 0.00007
NM_182914.3(SYNE2):c.19911C>T (p.Asn6637=) rs201444715 0.00006
NM_182914.3(SYNE2):c.303A>G (p.Leu101=) rs371277498 0.00006
NM_182914.3(SYNE2):c.1875C>T (p.His625=) rs372968718 0.00005
NM_182914.3(SYNE2):c.19962C>G (p.Leu6654=) rs139326092 0.00005
NM_182914.3(SYNE2):c.80-7T>G rs769250456 0.00005
NM_182914.3(SYNE2):c.16194C>T (p.Ala5398=) rs764264884 0.00004
NM_182914.3(SYNE2):c.17141G>A (p.Arg5714His) rs200137127 0.00004
NM_182914.3(SYNE2):c.9430C>T (p.Leu3144Phe) rs886044254 0.00004
NM_182914.3(SYNE2):c.12657G>A (p.Ala4219=) rs76668149 0.00003
NM_182914.3(SYNE2):c.12856A>C (p.Ile4286Leu) rs763081757 0.00003
NM_182914.3(SYNE2):c.16737G>A (p.Thr5579=) rs147156341 0.00003
NM_182914.3(SYNE2):c.2558C>G (p.Ser853Cys) rs763133096 0.00003
NM_182914.3(SYNE2):c.19272C>T (p.Asp6424=) rs774346816 0.00002
NM_182914.3(SYNE2):c.15921G>T (p.Val5307=) rs555313966 0.00001
NM_182914.3(SYNE2):c.16602C>G (p.Phe5534Leu) rs748802577 0.00001
NM_182914.3(SYNE2):c.19023C>A (p.Ser6341=) rs759765636 0.00001
NM_182914.3(SYNE2):c.1914C>T (p.Val638=) rs756044885 0.00001
NM_182914.3(SYNE2):c.19497T>C (p.Val6499=) rs1176808345 0.00001
NM_182914.3(SYNE2):c.6742G>A (p.Val2248Ile) rs767605722 0.00001
NM_182914.3(SYNE2):c.10248G>A (p.Glu3416=)
NM_182914.3(SYNE2):c.10860A>G (p.Gln3620=)
NM_182914.3(SYNE2):c.11001T>C (p.Ala3667=)
NM_182914.3(SYNE2):c.11835T>G (p.Ala3945=)
NM_182914.3(SYNE2):c.11994C>T (p.Thr3998=)
NM_182914.3(SYNE2):c.12301C>T (p.Arg4101Trp)
NM_182914.3(SYNE2):c.14831A>C (p.Lys4944Thr)
NM_182914.3(SYNE2):c.15316A>G (p.Met5106Val) rs376851893
NM_182914.3(SYNE2):c.15572A>G (p.Glu5191Gly)
NM_182914.3(SYNE2):c.16404C>T (p.Leu5468=)
NM_182914.3(SYNE2):c.16572C>T (p.His5524=) rs746969779
NM_182914.3(SYNE2):c.16798T>C (p.Tyr5600His)
NM_182914.3(SYNE2):c.17707T>C (p.Leu5903=)
NM_182914.3(SYNE2):c.18190G>A (p.Ala6064Thr) rs182079744
NM_182914.3(SYNE2):c.18282C>A (p.Ser6094=)
NM_182914.3(SYNE2):c.18852C>A (p.Arg6284=)
NM_182914.3(SYNE2):c.19515G>A (p.Ala6505=)
NM_182914.3(SYNE2):c.201C>T (p.Leu67=)
NM_182914.3(SYNE2):c.20442A>G (p.Ala6814=)
NM_182914.3(SYNE2):c.2904T>C (p.Arg968=)
NM_182914.3(SYNE2):c.3087T>C (p.Leu1029=)
NM_182914.3(SYNE2):c.3354G>A (p.Arg1118=)
NM_182914.3(SYNE2):c.4196G>A (p.Cys1399Tyr)
NM_182914.3(SYNE2):c.4362T>C (p.Gly1454=)
NM_182914.3(SYNE2):c.589A>T (p.Thr197Ser)
NM_182914.3(SYNE2):c.606T>C (p.Asn202=)
NM_182914.3(SYNE2):c.6296C>A (p.Thr2099Asn)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.