ClinVar Miner

List of variants reported as likely benign for Adams-Oliver syndrome 1 by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 58
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HGVS dbSNP
NM_020754.4(ARHGAP31):c.*105T>C rs185124298
NM_020754.4(ARHGAP31):c.*1126A>T rs116466342
NM_020754.4(ARHGAP31):c.*1156C>G rs115630304
NM_020754.4(ARHGAP31):c.*1176T>G rs114261128
NM_020754.4(ARHGAP31):c.*1219C>T rs113918185
NM_020754.4(ARHGAP31):c.*1238T>C rs115845847
NM_020754.4(ARHGAP31):c.*1311A>T rs146808640
NM_020754.4(ARHGAP31):c.*1386A>T rs180781573
NM_020754.4(ARHGAP31):c.*1387_*1390CTCA[1] rs201595453
NM_020754.4(ARHGAP31):c.*1533T>C rs567101775
NM_020754.4(ARHGAP31):c.*1657C>T rs78943363
NM_020754.4(ARHGAP31):c.*1692G>T rs76616804
NM_020754.4(ARHGAP31):c.*1987C>G rs559362755
NM_020754.4(ARHGAP31):c.*1995G>A rs186689946
NM_020754.4(ARHGAP31):c.*2051C>A rs74665630
NM_020754.4(ARHGAP31):c.*2173G>A rs534303032
NM_020754.4(ARHGAP31):c.*2192G>T rs566368695
NM_020754.4(ARHGAP31):c.*2281C>G rs183825811
NM_020754.4(ARHGAP31):c.*267C>T rs3732415
NM_020754.4(ARHGAP31):c.*2689C>T rs529808528
NM_020754.4(ARHGAP31):c.*2743C>A rs78013508
NM_020754.4(ARHGAP31):c.*2802G>A rs77420174
NM_020754.4(ARHGAP31):c.*2842T>C rs147003993
NM_020754.4(ARHGAP31):c.*3021G>A rs116075883
NM_020754.4(ARHGAP31):c.*3123A>G rs574039254
NM_020754.4(ARHGAP31):c.*3166C>G rs138144745
NM_020754.4(ARHGAP31):c.*466C>T rs116944967
NM_020754.4(ARHGAP31):c.*590C>T rs145064712
NM_020754.4(ARHGAP31):c.-149G>A rs62265186
NM_020754.4(ARHGAP31):c.-295A>G rs549187231
NM_020754.4(ARHGAP31):c.-369G>A rs548441120
NM_020754.4(ARHGAP31):c.-40G>A rs149723943
NM_020754.4(ARHGAP31):c.100+9C>T rs76783588
NM_020754.4(ARHGAP31):c.1178A>G (p.Lys393Arg) rs574813801
NM_020754.4(ARHGAP31):c.1430C>T (p.Pro477Leu) rs200233879
NM_020754.4(ARHGAP31):c.1618A>G (p.Lys540Glu) rs61744410
NM_020754.4(ARHGAP31):c.1926+13C>A rs140274779
NM_020754.4(ARHGAP31):c.203+6C>T rs141911639
NM_020754.4(ARHGAP31):c.2036C>T (p.Thr679Ile) rs61736796
NM_020754.4(ARHGAP31):c.2180C>T (p.Thr727Ile) rs539048828
NM_020754.4(ARHGAP31):c.2359C>G (p.Pro787Ala) rs186621177
NM_020754.4(ARHGAP31):c.2814G>T (p.Gln938His) rs201519258
NM_020754.4(ARHGAP31):c.3104C>T (p.Thr1035Ile) rs201997376
NM_020754.4(ARHGAP31):c.3458A>G (p.Asp1153Gly) rs184040818
NM_020754.4(ARHGAP31):c.349-7T>G rs200397968
NM_020754.4(ARHGAP31):c.3801C>T (p.Pro1267=) rs200959673
NM_020754.4(ARHGAP31):c.3802G>A (p.Gly1268Arg) rs149658506
NM_020754.4(ARHGAP31):c.384G>C (p.Leu128=) rs150339878
NM_020754.4(ARHGAP31):c.3953G>T (p.Gly1318Val) rs529703977
NM_020754.4(ARHGAP31):c.3983G>A (p.Arg1328Gln) rs199708581
NM_020754.4(ARHGAP31):c.4096G>A (p.Val1366Met) rs3796360
NM_020754.4(ARHGAP31):c.4110G>A (p.Lys1370=) rs76054211
NM_020754.4(ARHGAP31):c.4132A>G (p.Ser1378Gly) rs193198313
NM_020754.4(ARHGAP31):c.432-7A>G rs10049221
NM_020754.4(ARHGAP31):c.435C>G (p.Thr145=) rs201927115
NM_020754.4(ARHGAP31):c.662C>T (p.Pro221Leu) rs751793
NM_020754.4(ARHGAP31):c.820C>T (p.Pro274Ser) rs139600783
NM_020754.4(ARHGAP31):c.936T>C (p.Arg312=) rs200813566

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