ClinVar Miner

List of variants in gene RAB3GAP1, ZRANB3 studied for Warburg micro syndrome

Included ClinVar conditions (6):
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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_001172435.1(RAB3GAP1):c.*1941G>T rs2305247
NM_012233.3(RAB3GAP1):c.*1056G>A
NM_012233.3(RAB3GAP1):c.*1077T>C rs16831395
NM_012233.3(RAB3GAP1):c.*1107A>C
NM_012233.3(RAB3GAP1):c.*1208del rs200869351
NM_012233.3(RAB3GAP1):c.*1208dup rs200869351
NM_012233.3(RAB3GAP1):c.*1209T>C
NM_012233.3(RAB3GAP1):c.*1212A>G
NM_012233.3(RAB3GAP1):c.*1247T>C
NM_012233.3(RAB3GAP1):c.*1272T>C
NM_012233.3(RAB3GAP1):c.*135C>G rs10170125
NM_012233.3(RAB3GAP1):c.*1378T>C rs59746814
NM_012233.3(RAB3GAP1):c.*1397C>T rs147177352
NM_012233.3(RAB3GAP1):c.*1511G>A rs575731807
NM_012233.3(RAB3GAP1):c.*1534G>A
NM_012233.3(RAB3GAP1):c.*1543T>C
NM_012233.3(RAB3GAP1):c.*1611A>T rs188370805
NM_012233.3(RAB3GAP1):c.*1693G>C rs144378327
NM_012233.3(RAB3GAP1):c.*170C>T rs180839370
NM_012233.3(RAB3GAP1):c.*171G>A rs11558413
NM_012233.3(RAB3GAP1):c.*174T>C rs886054854
NM_012233.3(RAB3GAP1):c.*1764C>G
NM_012233.3(RAB3GAP1):c.*1826G>C
NM_012233.3(RAB3GAP1):c.*1898G>A
NM_012233.3(RAB3GAP1):c.*201T>G rs78044288
NM_012233.3(RAB3GAP1):c.*252T>G rs7564565
NM_012233.3(RAB3GAP1):c.*255T>G
NM_012233.3(RAB3GAP1):c.*261dup rs143703110
NM_012233.3(RAB3GAP1):c.*283C>T rs765003230
NM_012233.3(RAB3GAP1):c.*303G>A rs72980321
NM_012233.3(RAB3GAP1):c.*324T>G rs886054855
NM_012233.3(RAB3GAP1):c.*346G>A rs534792972
NM_012233.3(RAB3GAP1):c.*404C>T rs149483456
NM_012233.3(RAB3GAP1):c.*507A>G
NM_012233.3(RAB3GAP1):c.*547A>G rs886054856
NM_012233.3(RAB3GAP1):c.*557T>C
NM_012233.3(RAB3GAP1):c.*647T>C
NM_012233.3(RAB3GAP1):c.*822T>G
NM_012233.3(RAB3GAP1):c.*985dup rs370069043
NM_012233.3(RAB3GAP1):c.*992G>A
NM_012233.3(RAB3GAP1):c.*995T>C rs116237324
NM_012233.3(RAB3GAP1):c.2642T>G (p.Leu881Ter) rs797045905
NM_012233.3(RAB3GAP1):c.2800C>A (p.Pro934Thr)
NM_012233.3(RAB3GAP1):c.2800C>G (p.Pro934Ala) rs77535003
NM_012233.3(RAB3GAP1):c.2801del (p.Pro934fs) rs730882182
NM_012233.3(RAB3GAP1):c.2831C>A (p.Thr944Asn)
NM_012233.3(RAB3GAP1):c.2839C>T (p.Arg947Cys) rs751620093
NM_012233.3(RAB3GAP1):c.2865_2866insTTCT (p.Pro956fs) rs1553450718
NM_012233.3(RAB3GAP1):c.2946A>G (p.Ter982Trp) rs141436429

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