ClinVar Miner

List of variants in gene COL11A1 reported as uncertain significance by GeneDx

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Total variants: 29
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HGVS dbSNP
NM_001854.4(COL11A1):c.1021G>C (p.Glu341Gln) rs144884147
NM_001854.4(COL11A1):c.1039G>A (p.Asp347Asn) rs199942159
NM_001854.4(COL11A1):c.1063T>C (p.Ser355Pro) rs141036911
NM_001854.4(COL11A1):c.1155A>C (p.Glu385Asp) rs1057524404
NM_001854.4(COL11A1):c.1201T>A (p.Phe401Ile) rs141817156
NM_001854.4(COL11A1):c.1427G>A (p.Arg476His) rs149558726
NM_001854.4(COL11A1):c.1444G>A (p.Ala482Thr) rs150428394
NM_001854.4(COL11A1):c.146A>G (p.Asn49Ser) rs145159429
NM_001854.4(COL11A1):c.1488G>A (p.Pro496=) rs772310071
NM_001854.4(COL11A1):c.168_170AAC[1] (p.Thr58del) rs1553253791
NM_001854.4(COL11A1):c.173C>T (p.Thr58Met) rs770162224
NM_001854.4(COL11A1):c.1961T>C (p.Leu654Pro) rs1131691449
NM_001854.4(COL11A1):c.2470G>A (p.Asp824Asn) rs1064796668
NM_001854.4(COL11A1):c.2725G>A (p.Asp909Asn) rs779028602
NM_001854.4(COL11A1):c.2921C>A (p.Pro974Gln) rs78046647
NM_001854.4(COL11A1):c.328G>C (p.Gly110Arg) rs141978499
NM_001854.4(COL11A1):c.3358G>A (p.Gly1120Ser) rs370589018
NM_001854.4(COL11A1):c.3652A>G (p.Met1218Val) rs951017335
NM_001854.4(COL11A1):c.3831A>C (p.Glu1277Asp) rs780739712
NM_001854.4(COL11A1):c.3868G>T (p.Ala1290Ser) rs370988085
NM_001854.4(COL11A1):c.4057G>A (p.Ala1353Thr) rs151249006
NM_001854.4(COL11A1):c.4100C>T (p.Ala1367Val) rs1057518442
NM_001854.4(COL11A1):c.4411G>A (p.Gly1471Ser) rs1057522949
NM_001854.4(COL11A1):c.4526A>C (p.Gln1509Pro) rs1057521422
NM_001854.4(COL11A1):c.4552A>C (p.Thr1518Pro) rs1057523166
NM_001854.4(COL11A1):c.4661C>T (p.Thr1554Met) rs759287748
NM_001854.4(COL11A1):c.4718C>T (p.Ser1573Leu) rs143531636
NM_001854.4(COL11A1):c.4802C>A (p.Thr1601Asn) rs143206624
NM_001854.4(COL11A1):c.973G>T (p.Val325Phe) rs746633493

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