ClinVar Miner

List of variants in gene PALLD reported as uncertain significance for Pancreatic cancer, susceptibility to, 1

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.-83+9G>A rs150719521 0.00037
NM_001166108.2(PALLD):c.-143A>G rs571957605 0.00024
NM_001166108.2(PALLD):c.-115C>G rs189011214 0.00011
NM_001166108.2(PALLD):c.-135A>G rs540285834 0.00009
NM_001166108.2(PALLD):c.2084T>G (p.Leu695Arg) rs139375029 0.00006
NM_001166108.2(PALLD):c.428G>A (p.Arg143His) rs149345491 0.00006
NM_001166108.2(PALLD):c.1433G>A (p.Gly478Glu) rs201816881 0.00004
NM_001166108.2(PALLD):c.556G>A (p.Ala186Thr) rs139434937 0.00003
NM_001166108.2(PALLD):c.860G>A (p.Arg287Gln) rs141283998 0.00002
NM_001166108.2(PALLD):c.-172C>A rs777479051 0.00001
NM_001166108.2(PALLD):c.-178G>A rs886059207 0.00001
NM_001166108.2(PALLD):c.107A>G (p.Gln36Arg) rs889514388 0.00001
NM_001166108.2(PALLD):c.1129A>G (p.Lys377Glu) rs368684220 0.00001
NM_001166108.2(PALLD):c.1219A>T (p.Thr407Ser) rs775730191 0.00001
NM_001166108.2(PALLD):c.1260+8T>C rs887513464 0.00001
NM_001166108.2(PALLD):c.2057G>A (p.Arg686Gln) rs1031710807 0.00001
NM_001166108.2(PALLD):c.2099C>T (p.Pro700Leu) rs1255873290 0.00001
NM_001166108.2(PALLD):c.222C>T (p.Ser74=) rs201038000 0.00001
NM_001166108.2(PALLD):c.836G>C (p.Ser279Thr) rs886059209 0.00001
NM_001166108.2(PALLD):c.1135A>G (p.Arg379Gly)
NM_001166108.2(PALLD):c.1155-16C>A
NM_001166108.2(PALLD):c.1266C>G (p.His422Gln)
NM_001166108.2(PALLD):c.1268G>T (p.Ser423Ile)
NM_001166108.2(PALLD):c.1412A>T (p.Gln471Leu)
NM_001166108.2(PALLD):c.1502-9C>T
NM_001166108.2(PALLD):c.1571G>T (p.Arg524Ile) rs776908136
NM_001166108.2(PALLD):c.1616C>T (p.Thr539Ile) rs780510622
NM_001166108.2(PALLD):c.164C>A (p.Thr55Lys)
NM_001166108.2(PALLD):c.1811A>G (p.Asn604Ser)
NM_001166108.2(PALLD):c.1850G>A (p.Arg617His)
NM_001166108.2(PALLD):c.1926C>G (p.Pro642=) rs886059210
NM_001166108.2(PALLD):c.1942C>T (p.Pro648Ser)
NM_001166108.2(PALLD):c.1957C>A (p.Pro653Thr) rs1784873065
NM_001166108.2(PALLD):c.2027C>A (p.Thr676Lys)
NM_001166108.2(PALLD):c.2063T>G (p.Leu688Arg)
NM_001166108.2(PALLD):c.215C>T (p.Pro72Leu)
NM_001166108.2(PALLD):c.236C>G (p.Pro79Arg)
NM_001166108.2(PALLD):c.301C>T (p.Pro101Ser)
NM_001166108.2(PALLD):c.349G>T (p.Val117Phe)
NM_001166108.2(PALLD):c.34G>A (p.Asp12Asn)
NM_001166108.2(PALLD):c.569A>G (p.Asn190Ser)
NM_001166108.2(PALLD):c.574A>G (p.Ser192Gly) rs1762575507
NM_001166108.2(PALLD):c.593C>T (p.Ser198Leu)
NM_001166108.2(PALLD):c.622A>G (p.Lys208Glu)
NM_001166108.2(PALLD):c.639C>A (p.Ala213=) rs1762581096
NM_001166108.2(PALLD):c.721C>T (p.His241Tyr) rs1490249027
NM_001166108.2(PALLD):c.815G>A (p.Arg272Gln)
NM_001166108.2(PALLD):c.855G>T (p.Gly285=)
NM_001166108.2(PALLD):c.876_877insCTGG (p.Arg293fs)
NM_001166108.2(PALLD):c.908+3A>G rs1762604026
NM_001166108.2(PALLD):c.946G>T (p.Asp316Tyr) rs1477916241

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