ClinVar Miner

List of variants in gene TCTN3 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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NM_015631.6(TCTN3):c.1013A>G (p.Lys338Arg)
NM_015631.6(TCTN3):c.1059C>T (p.Gly353=)
NM_015631.6(TCTN3):c.1177G>A (p.Ala393Thr)
NM_015631.6(TCTN3):c.1196G>A (p.Ser399Asn) rs768285987
NM_015631.6(TCTN3):c.1271T>G (p.Val424Gly) rs200705429
NM_015631.6(TCTN3):c.1741G>C (p.Val581Leu)
NM_015631.6(TCTN3):c.283A>C (p.Thr95Pro) rs749447795
NM_015631.6(TCTN3):c.606A>G (p.Gln202=)
NM_015631.6(TCTN3):c.728A>G (p.Asn243Ser) rs1555270274
NM_015631.6(TCTN3):c.730C>G (p.Pro244Ala)
NM_015631.6(TCTN3):c.769C>T (p.Arg257Cys)
NM_015631.6(TCTN3):c.818A>G (p.Asn273Ser) rs762720849
NM_015631.6(TCTN3):c.883A>G (p.Met295Val)

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