ClinVar Miner

List of variants in gene PALB2 studied for Carcinoma of colon

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.2234A>G (p.Lys745Arg) rs142343372 0.00005
NM_024675.4(PALB2):c.3404G>A (p.Gly1135Glu) rs730881894 0.00005
NM_024675.4(PALB2):c.2067G>A (p.Ser689=) rs371149159 0.00004
NM_024675.4(PALB2):c.829G>A (p.Asp277Asn) rs778309339 0.00004
NM_024675.4(PALB2):c.1766C>T (p.Thr589Met) rs773340677 0.00003
NM_024675.4(PALB2):c.226A>G (p.Ile76Val) rs541028076 0.00003
NM_024675.4(PALB2):c.2360C>T (p.Thr787Ile) rs201042302 0.00002
NM_024675.4(PALB2):c.1610C>T (p.Ser537Leu) rs142103232 0.00001
NM_024675.4(PALB2):c.1720T>C (p.Ser574Pro) rs1214293842 0.00001
NM_024675.4(PALB2):c.2750T>C (p.Val917Ala) rs763645981 0.00001
NM_024675.4(PALB2):c.2971G>T (p.Val991Phe) rs765175665 0.00001
NM_024675.4(PALB2):c.3106G>C (p.Val1036Leu) rs756906403 0.00001
NM_024675.4(PALB2):c.3232T>A (p.Cys1078Ser) rs876659587 0.00001
NM_024675.4(PALB2):c.1399G>A (p.Gly467Ser) rs45602239
NM_024675.4(PALB2):c.1454C>T (p.Thr485Ile) rs786202699
NM_024675.4(PALB2):c.1537A>G (p.Thr513Ala) rs1060502741
NM_024675.4(PALB2):c.1881G>T (p.Val627=) rs139362268
NM_024675.4(PALB2):c.21G>T (p.Lys7Asn) rs1424944402
NM_024675.4(PALB2):c.227T>C (p.Ile76Thr) rs1967061407
NM_024675.4(PALB2):c.247C>A (p.His83Asn) rs773732106
NM_024675.4(PALB2):c.2999G>A (p.Gly1000Asp) rs1597079946
NM_024675.4(PALB2):c.3026C>T (p.Pro1009Leu) rs552354535
NM_024675.4(PALB2):c.3103A>T (p.Ile1035Phe) rs863224783
NM_024675.4(PALB2):c.364G>A (p.Asp122Asn) rs730881880
NM_024675.4(PALB2):c.892_893del (p.Val298fs) rs2142431841
NM_024675.4(PALB2):c.941A>G (p.Gln314Arg) rs2142430398

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