ClinVar Miner

List of variants in gene PRICKLE1 reported as uncertain significance for not provided

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Total variants: 56
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HGVS dbSNP
NM_153026.3(PRICKLE1):c.100G>A (p.Ala34Thr) rs781255236
NM_153026.3(PRICKLE1):c.101C>T (p.Ala34Val) rs139176541
NM_153026.3(PRICKLE1):c.1108A>G (p.Thr370Ala)
NM_153026.3(PRICKLE1):c.113C>T (p.Pro38Leu) rs145493619
NM_153026.3(PRICKLE1):c.1145G>A (p.Arg382Lys) rs748636455
NM_153026.3(PRICKLE1):c.114G>A (p.Pro38=) rs141743294
NM_153026.3(PRICKLE1):c.1198G>C (p.Glu400Gln) rs796052931
NM_153026.3(PRICKLE1):c.1222T>C (p.Trp408Arg) rs376384105
NM_153026.3(PRICKLE1):c.1243A>G (p.Met415Val) rs776720321
NM_153026.3(PRICKLE1):c.1248G>A (p.Thr416=) rs142502371
NM_153026.3(PRICKLE1):c.1318A>G (p.Ser440Gly) rs1566080286
NM_153026.3(PRICKLE1):c.1324C>T (p.His442Tyr) rs1420840004
NM_153026.3(PRICKLE1):c.132G>A (p.Gln44=) rs377668062
NM_153026.3(PRICKLE1):c.1360G>A (p.Glu454Lys) rs748454609
NM_153026.3(PRICKLE1):c.1435G>A (p.Gly479Arg) rs570770626
NM_153026.3(PRICKLE1):c.1444G>A (p.Asp482Asn) rs1555229983
NM_153026.3(PRICKLE1):c.1461C>T (p.Ser487=) rs116197349
NM_153026.3(PRICKLE1):c.1516G>A (p.Ala506Thr) rs796052932
NM_153026.3(PRICKLE1):c.1547G>C (p.Trp516Ser) rs139901494
NM_153026.3(PRICKLE1):c.1601G>A (p.Arg534Gln) rs756192425
NM_153026.3(PRICKLE1):c.1676C>T (p.Ser559Leu) rs771584708
NM_153026.3(PRICKLE1):c.1699_1701GAG[1] (p.Glu568del) rs1413929405
NM_153026.3(PRICKLE1):c.1888C>G (p.Gln630Glu) rs200171609
NM_153026.3(PRICKLE1):c.1922G>A (p.Gly641Glu) rs374621616
NM_153026.3(PRICKLE1):c.1942C>G (p.Arg648Gly) rs370129051
NM_153026.3(PRICKLE1):c.1960G>A (p.Glu654Lys) rs1555229356
NM_153026.3(PRICKLE1):c.2002T>A (p.Ser668Thr) rs794727934
NM_153026.3(PRICKLE1):c.2027G>A (p.Arg676Gln) rs377294908
NM_153026.3(PRICKLE1):c.2037A>C (p.Arg679Ser) rs1057520141
NM_153026.3(PRICKLE1):c.2043C>T (p.Ser681=) rs1555229314
NM_153026.3(PRICKLE1):c.2071A>G (p.Thr691Ala) rs149496604
NM_153026.3(PRICKLE1):c.2105G>A (p.Arg702Gln) rs369790443
NM_153026.3(PRICKLE1):c.2167G>A (p.Ala723Thr) rs796052933
NM_153026.3(PRICKLE1):c.2216C>T (p.Ser739Phe) rs138452760
NM_153026.3(PRICKLE1):c.2224G>A (p.Gly742Ser) rs370967125
NM_153026.3(PRICKLE1):c.2262C>G (p.Leu754=) rs727504104
NM_153026.3(PRICKLE1):c.2269G>A (p.Glu757Lys) rs145860632
NM_153026.3(PRICKLE1):c.2275G>A (p.Asp759Asn) rs886042287
NM_153026.3(PRICKLE1):c.2288G>A (p.Cys763Tyr) rs886044288
NM_153026.3(PRICKLE1):c.2330A>G (p.Tyr777Cys) rs768039518
NM_153026.3(PRICKLE1):c.2404C>T (p.Pro802Ser) rs150545495
NM_153026.3(PRICKLE1):c.25A>G (p.Met9Val) rs566073131
NM_153026.3(PRICKLE1):c.384+6C>A
NM_153026.3(PRICKLE1):c.391T>G (p.Leu131Val) rs35731866
NM_153026.3(PRICKLE1):c.425C>T (p.Ala142Val) rs796052928
NM_153026.3(PRICKLE1):c.431G>A (p.Arg144His) rs281865563
NM_153026.3(PRICKLE1):c.434C>T (p.Ala145Val) rs765119777
NM_153026.3(PRICKLE1):c.626G>A (p.Arg209His) rs758400992
NM_153026.3(PRICKLE1):c.668C>T (p.Thr223Met) rs754218148
NM_153026.3(PRICKLE1):c.703G>A (p.Gly235Ser) rs375197568
NM_153026.3(PRICKLE1):c.713T>C (p.Phe238Ser) rs796052930
NM_153026.3(PRICKLE1):c.808C>A (p.Gln270Lys) rs752070986
NM_153026.3(PRICKLE1):c.824C>T (p.Thr275Met) rs559947948
NM_153026.3(PRICKLE1):c.853A>C (p.Lys285Gln) rs1555230175
NM_153026.3(PRICKLE1):c.910A>G (p.Lys304Glu) rs202205425
NM_153026.3(PRICKLE1):c.920G>A (p.Ser307Asn) rs886043436

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