ClinVar Miner

List of variants in gene LOC106736614, RET studied for carcinoma

Included ClinVar conditions (242):
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.-2C>A rs876657980 0.00049
NM_020975.6(RET):c.-37G>C rs751005619 0.00004
NM_020975.6(RET):c.6G>A (p.Ala2=) rs1243883489 0.00004
NM_020975.6(RET):c.31C>A (p.Leu11Met) rs587780812 0.00003
NM_020975.6(RET):c.30G>A (p.Gly10=) rs1050242868 0.00002
NM_020975.6(RET):c.15G>C (p.Thr5=) rs1226499208 0.00001
NM_020975.6(RET):c.18C>T (p.Ser6=) rs1185431356 0.00001
NM_020975.6(RET):c.19G>A (p.Gly7Ser) rs1257661718 0.00001
NM_020630.5(RET):c.-234_-230dup rs386134265
NM_020975.6(RET):c.10G>A (p.Ala4Thr) rs1837063785
NM_020975.6(RET):c.11C>T (p.Ala4Val) rs1837063876
NM_020975.6(RET):c.13A>G (p.Thr5Ala)
NM_020975.6(RET):c.14C>G (p.Thr5Arg) rs1444096302
NM_020975.6(RET):c.14C>T (p.Thr5Met) rs1444096302
NM_020975.6(RET):c.15G>A (p.Thr5=)
NM_020975.6(RET):c.16T>C (p.Ser6Pro) rs1588848475
NM_020975.6(RET):c.16T>G (p.Ser6Ala) rs1588848475
NM_020975.6(RET):c.19G>C (p.Gly7Arg)
NM_020975.6(RET):c.20G>A (p.Gly7Asp) rs1366681125
NM_020975.6(RET):c.20G>T (p.Gly7Val) rs1366681125
NM_020975.6(RET):c.22G>T (p.Ala8Ser) rs1476325851
NM_020975.6(RET):c.28G>A (p.Gly10Arg)
NM_020975.6(RET):c.29G>A (p.Gly10Glu) rs1303812507
NM_020975.6(RET):c.29G>C (p.Gly10Ala) rs1303812507
NM_020975.6(RET):c.29G>T (p.Gly10Val) rs1303812507
NM_020975.6(RET):c.30G>T (p.Gly10=) rs1050242868
NM_020975.6(RET):c.31C>G (p.Leu11Val) rs587780812
NM_020975.6(RET):c.31C>T (p.Leu11=) rs587780812
NM_020975.6(RET):c.35_52dup (p.Leu17_Leu18insArgLeuLeuLeuLeuLeu) rs1837065209
NM_020975.6(RET):c.35_55dup (p.Leu18_Leu19insArgLeuLeuLeuLeuLeuLeu) rs1467944441
NM_020975.6(RET):c.5C>A (p.Ala2Glu)
NM_020975.6(RET):c.5_28dup (p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla) rs1837063549
NM_020975.6(RET):c.6G>T (p.Ala2=)
NM_020975.6(RET):c.7A>G (p.Lys3Glu) rs1564480827

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