ClinVar Miner

List of variants reported as benign for Baller-Gerold syndrome by Invitae

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_004260.3(RECQL4):c.1090G>A (p.Val364Met) rs144637135
NM_004260.3(RECQL4):c.1258+6A>T rs34437789
NM_004260.3(RECQL4):c.1390+3G>A rs148912524
NM_004260.3(RECQL4):c.1395G>A (p.Thr465=) rs34948955
NM_004260.3(RECQL4):c.1398G>A (p.Pro466=) rs145615931
NM_004260.3(RECQL4):c.1564C>T (p.Arg522Cys) rs35407712
NM_004260.3(RECQL4):c.1565G>A (p.Arg522His) rs35842750
NM_004260.3(RECQL4):c.161A>G (p.Gln54Arg) rs35198096
NM_004260.3(RECQL4):c.1621-8A>G rs373357384
NM_004260.3(RECQL4):c.1625C>T (p.Ser542Phe) rs369852601
NM_004260.3(RECQL4):c.1704+9C>T rs35876881
NM_004260.3(RECQL4):c.171C>T (p.Gly57=) rs758179747
NM_004260.3(RECQL4):c.1772C>T (p.Pro591Leu) rs2721191
NM_004260.3(RECQL4):c.1899C>T (p.Gly633=) rs557065974
NM_004260.3(RECQL4):c.1954G>A (p.Val652Met) rs61754061
NM_004260.3(RECQL4):c.1959A>G (p.Ala653=) rs574411332
NM_004260.3(RECQL4):c.195C>G (p.Leu65=) rs369163654
NM_004260.3(RECQL4):c.2059-8_2059-6delCTC rs558061753
NM_004260.3(RECQL4):c.212A>G (p.Glu71Gly) rs34642881
NM_004260.3(RECQL4):c.2131G>A (p.Glu711Lys) rs371818842
NM_004260.3(RECQL4):c.2223C>T (p.Ala741=) rs34271972
NM_004260.3(RECQL4):c.2238G>A (p.Ala746=) rs35215952
NM_004260.3(RECQL4):c.2377C>T (p.Pro793Ser) rs35098923
NM_004260.3(RECQL4):c.2395G>A (p.Val799Met) rs34293591
NM_004260.3(RECQL4):c.2415C>T (p.Ala805=) rs34735741
NM_004260.3(RECQL4):c.2460C>T (p.Pro820=) rs202078917
NM_004260.3(RECQL4):c.2463+6C>T rs35029361
NM_004260.3(RECQL4):c.2463+7del rs760575376
NM_004260.3(RECQL4):c.2544C>T (p.Arg848=) rs200114521
NM_004260.3(RECQL4):c.2569_2574delTGCACC (p.Cys857_Thr858del) rs548804317
NM_004260.3(RECQL4):c.2569_2574dup (p.Thr858_Arg859insCysThr) rs548804317
NM_004260.3(RECQL4):c.2601C>G (p.Ala867=) rs34358597
NM_004260.3(RECQL4):c.2636C>A (p.Pro879His) rs137975310
NM_004260.3(RECQL4):c.274C>T (p.Pro92Ser) rs2721190
NM_004260.3(RECQL4):c.275C>T (p.Pro92Leu) rs200516441
NM_004260.3(RECQL4):c.2817G>A (p.Ala939=) rs202045203
NM_004260.3(RECQL4):c.300C>T (p.Gly100=) rs34496005
NM_004260.3(RECQL4):c.3058G>A (p.Val1020Met) rs114149451
NM_004260.3(RECQL4):c.3062G>A (p.Arg1021Gln) rs34666647
NM_004260.3(RECQL4):c.309G>A (p.Pro103=) rs4251688
NM_004260.3(RECQL4):c.3127C>T (p.Leu1043=) rs4925828
NM_004260.3(RECQL4):c.3133G>A (p.Ala1045Thr) rs35348691
NM_004260.3(RECQL4):c.3313G>A (p.Gly1105Ser) rs34915097
NM_004260.3(RECQL4):c.3314G>A (p.Gly1105Asp) rs36078464
NM_004260.3(RECQL4):c.3337G>C (p.Gly1113Arg) rs35101495
NM_004260.3(RECQL4):c.3392G>A (p.Arg1131Lys) rs201369291
NM_004260.3(RECQL4):c.3393+8_3393+9delCAinsTG rs878854649
NM_004260.3(RECQL4):c.3435G>C (p.Gln1145His) rs61755066
NM_004260.3(RECQL4):c.3443C>T (p.Ser1148Phe) rs35346077
NM_004260.3(RECQL4):c.3480G>A (p.Val1160=) rs34914400
NM_004260.3(RECQL4):c.3531C>T (p.Tyr1177=) rs139228543
NM_004260.3(RECQL4):c.3563T>C (p.Leu1188Pro) rs535259922
NM_004260.3(RECQL4):c.3573C>T (p.Ser1191=) rs199885535
NM_004260.3(RECQL4):c.3594G>A (p.Leu1198=) rs146398243
NM_004260.3(RECQL4):c.3609C>T (p.Leu1203=) rs201384843
NM_004260.3(RECQL4):c.465C>G (p.Val155=) rs116137512
NM_004260.3(RECQL4):c.492G>A (p.Glu164=) rs368335924
NM_004260.3(RECQL4):c.543G>A (p.Gln181=) rs34159914
NM_004260.3(RECQL4):c.565G>A (p.Gly189Ser) rs34371341
NM_004260.3(RECQL4):c.615C>G (p.Pro205=) rs35639991
NM_004260.3(RECQL4):c.633T>C (p.Asp211=) rs571624962
NM_004260.3(RECQL4):c.716C>T (p.Ala239Val) rs146709578
NM_004260.3(RECQL4):c.755C>T (p.Pro252Leu) rs199773279
NM_004260.3(RECQL4):c.891C>T (p.Asp297=) rs34700133

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