ClinVar Miner

List of variants in gene combination LOC130004408, TCTN3 reported as likely benign for bone disorder

Included ClinVar conditions (1436):
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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_015631.6(TCTN3):c.159G>A (p.Ala53=) rs540555381 0.00011
NM_015631.6(TCTN3):c.25C>T (p.Leu9=) rs770794139 0.00010
NM_015631.6(TCTN3):c.165A>C (p.Ala55=) rs1385808173 0.00005
NM_015631.6(TCTN3):c.153A>G (p.Ser51=) rs937027387 0.00003
NM_015631.6(TCTN3):c.18C>T (p.Leu6=) rs879694012 0.00003
NM_015631.6(TCTN3):c.201C>T (p.Val67=) rs2097955925 0.00001
NM_015631.6(TCTN3):c.222G>A (p.Ser74=) rs913092788 0.00001
NM_015631.6(TCTN3):c.6C>A (p.Arg2=) rs1395472461 0.00001
NM_015631.6(TCTN3):c.9C>A (p.Thr3=) rs1471002377 0.00001
NM_015631.6(TCTN3):c.114G>T (p.Leu38=) rs1027956965
NM_015631.6(TCTN3):c.120A>G (p.Arg40=)
NM_015631.6(TCTN3):c.132C>T (p.Gly44=) rs1313346150
NM_015631.6(TCTN3):c.138C>T (p.Thr46=) rs887435654
NM_015631.6(TCTN3):c.159G>T (p.Ala53=) rs540555381
NM_015631.6(TCTN3):c.162T>A (p.Thr54=) rs1410663654
NM_015631.6(TCTN3):c.162T>C (p.Thr54=) rs1410663654
NM_015631.6(TCTN3):c.18C>G (p.Leu6=) rs879694012
NM_015631.6(TCTN3):c.198G>A (p.Val66=) rs1237516460
NM_015631.6(TCTN3):c.219C>T (p.Pro73=) rs752528883
NM_015631.6(TCTN3):c.21G>C (p.Ala7=) rs61737888
NM_015631.6(TCTN3):c.228T>G (p.Pro76=) rs1468519329
NM_015631.6(TCTN3):c.256+11A>G rs2492793416
NM_015631.6(TCTN3):c.256+7G>T
NM_015631.6(TCTN3):c.27G>A (p.Leu9=) rs973353630
NM_015631.6(TCTN3):c.27G>T (p.Leu9=) rs973353630
NM_015631.6(TCTN3):c.40C>T (p.Leu14=)
NM_015631.6(TCTN3):c.45G>T (p.Val15=)
NM_015631.6(TCTN3):c.51C>G (p.Pro17=) rs1482900802
NM_015631.6(TCTN3):c.51C>T (p.Pro17=)
NM_015631.6(TCTN3):c.57C>T (p.Gly19=) rs2492796188
NM_015631.6(TCTN3):c.78C>T (p.Ser26=) rs2492795939
NM_015631.6(TCTN3):c.9C>T (p.Thr3=)

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