ClinVar Miner

List of variants in gene VARS2 reported as likely benign for not provided

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Gene type:
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Total variants: 134
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HGVS dbSNP gnomAD frequency
NM_020442.6(VARS2):c.1075-70C>T rs118124843 0.01605
NM_020442.6(VARS2):c.1514C>T (p.Ser505Phe) rs61746524 0.01404
NM_020442.6(VARS2):c.1633-74C>T rs114889222 0.01024
NM_020442.6(VARS2):c.1670C>A (p.Ala557Asp) rs55822421 0.00736
NM_020442.6(VARS2):c.1074+38G>A rs146126712 0.00601
NM_020442.6(VARS2):c.671+247A>T rs560535786 0.00575
NM_020442.6(VARS2):c.423G>A (p.Met141Ile) rs141408930 0.00569
NM_020442.6(VARS2):c.2500C>T (p.Arg834Cys) rs142520878 0.00488
NM_020442.6(VARS2):c.2467-145T>C rs192670335 0.00463
NM_020442.6(VARS2):c.2673+150C>T rs144768058 0.00429
NM_020442.6(VARS2):c.607G>A (p.Gly203Arg) rs73430135 0.00342
NM_020442.6(VARS2):c.876G>A (p.Val292=) rs147636694 0.00332
NM_020442.6(VARS2):c.-27-81T>C rs193150789 0.00269
NM_020442.6(VARS2):c.1065G>A (p.Ser355=) rs151183326 0.00251
NM_020442.6(VARS2):c.969C>T (p.Pro323=) rs148701242 0.00214
NM_020442.6(VARS2):c.2551C>T (p.Arg851Cys) rs138855624 0.00129
NM_020442.6(VARS2):c.451T>C (p.Ser151Pro) rs150863068 0.00103
NM_020442.6(VARS2):c.2589G>C (p.Glu863Asp) rs143473050 0.00086
NM_020442.6(VARS2):c.874-7C>T rs148624317 0.00086
NM_020442.6(VARS2):c.672-16A>C rs202118530 0.00050
NM_020442.6(VARS2):c.864G>A (p.Ser288=) rs59234326 0.00043
NM_020442.6(VARS2):c.1691C>T (p.Ala564Val) rs143408155 0.00041
NM_020442.6(VARS2):c.3091-10C>T rs141974166 0.00041
NM_020442.6(VARS2):c.1074+15G>A rs200200291 0.00038
NM_020442.6(VARS2):c.2980A>G (p.Ile994Val) rs201758263 0.00038
NM_020442.6(VARS2):c.1074+9C>T rs375719143 0.00030
NM_020442.6(VARS2):c.2786-6T>C rs200168128 0.00028
NM_020442.6(VARS2):c.1338G>A (p.Leu446=) rs17189628 0.00026
NM_020442.6(VARS2):c.2704C>T (p.Arg902Cys) rs148172787 0.00020
NM_020442.6(VARS2):c.1083C>T (p.His361=) rs374035061 0.00017
NM_020442.6(VARS2):c.315C>T (p.Ser105=) rs199858134 0.00015
NM_020442.6(VARS2):c.1557-18C>T rs184580937 0.00011
NM_020442.6(VARS2):c.736T>C (p.Cys246Arg) rs140184279 0.00011
NM_020442.6(VARS2):c.2826C>T (p.Phe942=) rs769740013 0.00009
NM_020442.6(VARS2):c.283+3A>G rs367960344 0.00009
NM_020442.6(VARS2):c.1166-6C>T rs372991793 0.00007
NM_020442.6(VARS2):c.1233C>T (p.Ser411=) rs528281614 0.00005
NM_020442.6(VARS2):c.3091-3C>T rs76717439 0.00005
NM_020442.6(VARS2):c.873+7C>T rs761249902 0.00005
NM_020442.6(VARS2):c.3091-6G>A rs753415520 0.00004
NM_020442.6(VARS2):c.2535C>T (p.Cys845=) rs775824651 0.00002
NM_020442.6(VARS2):c.2785+13G>A rs577901199 0.00002
NM_020442.6(VARS2):c.573+13T>C rs376869444 0.00002
NM_020442.6(VARS2):c.1131C>T (p.Ile377=) rs1057522585 0.00001
NM_020442.6(VARS2):c.1653G>A (p.Val551=) rs760052413 0.00001
NM_020442.6(VARS2):c.18C>T (p.Leu6=) rs765761779 0.00001
NM_020442.6(VARS2):c.495C>T (p.Ala165=) rs1347356683 0.00001
NM_020442.6(VARS2):c.753+19G>C rs748007370 0.00001
NM_020442.6(VARS2):c.912A>G (p.Arg304=) rs773442834 0.00001
NC_000006.12:g.30914118_30914129del rs200449009
NM_020442.6(VARS2):c.-27-21C>G
NM_020442.6(VARS2):c.-27-21CT[4] rs745344704
NM_020442.6(VARS2):c.-27-21CT[7]
NM_020442.6(VARS2):c.-27-22G>A
NM_020442.6(VARS2):c.-27-9C>G
NM_020442.6(VARS2):c.1023G>A (p.Thr341=)
NM_020442.6(VARS2):c.105T>C (p.His35=)
NM_020442.6(VARS2):c.1066C>A (p.Arg356=) rs753139152
NM_020442.6(VARS2):c.1074+32C>T rs115947485
NM_020442.6(VARS2):c.1149G>A (p.Gln383=)
NM_020442.6(VARS2):c.1166-20C>A
NM_020442.6(VARS2):c.124A>C (p.Arg42=)
NM_020442.6(VARS2):c.1257T>C (p.Asp419=)
NM_020442.6(VARS2):c.1263C>T (p.Thr421=)
NM_020442.6(VARS2):c.1278C>T (p.Cys426=)
NM_020442.6(VARS2):c.1293+17T>C
NM_020442.6(VARS2):c.1294-17T>C
NM_020442.6(VARS2):c.1397+8C>A
NM_020442.6(VARS2):c.1398-107G>A rs9357103
NM_020442.6(VARS2):c.1512C>T (p.Pro504=)
NM_020442.6(VARS2):c.1556+15A>G
NM_020442.6(VARS2):c.1632+18C>A
NM_020442.6(VARS2):c.1633-16C>T
NM_020442.6(VARS2):c.1695A>G (p.Glu565=)
NM_020442.6(VARS2):c.1725C>T (p.Thr575=)
NM_020442.6(VARS2):c.180T>G (p.Ala60=)
NM_020442.6(VARS2):c.202-19T>C
NM_020442.6(VARS2):c.202-4T>C
NM_020442.6(VARS2):c.2457C>T (p.Asp819=)
NM_020442.6(VARS2):c.2466+14G>A
NM_020442.6(VARS2):c.2481C>T (p.Pro827=)
NM_020442.6(VARS2):c.2526G>A (p.Leu842=)
NM_020442.6(VARS2):c.2544C>T (p.Leu848=)
NM_020442.6(VARS2):c.2553C>T (p.Arg851=)
NM_020442.6(VARS2):c.2604G>A (p.Leu868=)
NM_020442.6(VARS2):c.2643G>A (p.Ser881=)
NM_020442.6(VARS2):c.2661C>T (p.Ser887=)
NM_020442.6(VARS2):c.2664C>T (p.Ala888=)
NM_020442.6(VARS2):c.2674-10C>G
NM_020442.6(VARS2):c.2674-9C>T
NM_020442.6(VARS2):c.2757G>A (p.Thr919=)
NM_020442.6(VARS2):c.2786-4C>G
NM_020442.6(VARS2):c.284-14C>G
NM_020442.6(VARS2):c.284-14C>T
NM_020442.6(VARS2):c.2886C>T (p.Pro962=)
NM_020442.6(VARS2):c.2889A>G (p.Pro963=)
NM_020442.6(VARS2):c.2907C>T (p.Ser969=)
NM_020442.6(VARS2):c.2961+10G>A
NM_020442.6(VARS2):c.3000C>T (p.Ala1000=)
NM_020442.6(VARS2):c.3036C>T (p.Ser1012=)
NM_020442.6(VARS2):c.3069A>G (p.Ala1023=)
NM_020442.6(VARS2):c.3151C>T (p.Leu1051=)
NM_020442.6(VARS2):c.3183G>A (p.Pro1061=)
NM_020442.6(VARS2):c.355C>A (p.Arg119=)
NM_020442.6(VARS2):c.383A>G (p.Gln128Arg)
NM_020442.6(VARS2):c.408G>A (p.Gly136=)
NM_020442.6(VARS2):c.477G>A (p.Thr159=)
NM_020442.6(VARS2):c.507-20_507-13del
NM_020442.6(VARS2):c.573+7_573+13dup
NM_020442.6(VARS2):c.574-27G>T rs139293635
NM_020442.6(VARS2):c.574-7A>C rs766933357
NM_020442.6(VARS2):c.574-7A>T
NM_020442.6(VARS2):c.582G>A (p.Val194=)
NM_020442.6(VARS2):c.592C>T (p.Leu198=)
NM_020442.6(VARS2):c.636G>A (p.Glu212=)
NM_020442.6(VARS2):c.63C>T (p.Gly21=)
NM_020442.6(VARS2):c.671+18G>T
NM_020442.6(VARS2):c.671+205GT[11] rs28383826
NM_020442.6(VARS2):c.671+205GT[15] rs28383826
NM_020442.6(VARS2):c.671+232TA[11] rs145049694
NM_020442.6(VARS2):c.671+232TA[12] rs145049694
NM_020442.6(VARS2):c.699G>A (p.Leu233=)
NM_020442.6(VARS2):c.69C>G (p.Pro23=) rs768525015
NM_020442.6(VARS2):c.754-18_754-10del
NM_020442.6(VARS2):c.789G>T (p.Arg263=) rs2150553294
NM_020442.6(VARS2):c.801G>A (p.Ala267=)
NM_020442.6(VARS2):c.81C>T (p.Ser27=)
NM_020442.6(VARS2):c.849A>G (p.Leu283=)
NM_020442.6(VARS2):c.855A>G (p.Ser285=)
NM_020442.6(VARS2):c.873+8G>A
NM_020442.6(VARS2):c.874-12C>T
NM_020442.6(VARS2):c.985+17G>T
NM_020442.6(VARS2):c.986-10T>C
NM_020442.6(VARS2):c.986-14A>C

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