ClinVar Miner

List of variants in gene TDRD7 reported as uncertain significance for cataract

Included ClinVar conditions (65):
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_014290.3(TDRD7):c.*191G>A rs185806845 0.00279
NM_014290.3(TDRD7):c.231C>T (p.Cys77=) rs143579801 0.00129
NM_014290.3(TDRD7):c.2488C>T (p.Arg830Cys) rs140697341 0.00086
NM_014290.3(TDRD7):c.189G>C (p.Glu63Asp) rs144477083 0.00046
NM_014290.3(TDRD7):c.2079+7C>T rs201253435 0.00035
NM_014290.3(TDRD7):c.2791C>T (p.Pro931Ser) rs146083361 0.00033
NM_014290.3(TDRD7):c.444C>T (p.Asn148=) rs144510531 0.00033
NM_014290.3(TDRD7):c.2665A>G (p.Met889Val) rs149536158 0.00029
NM_014290.3(TDRD7):c.622A>G (p.Thr208Ala) rs139706467 0.00029
NM_014290.3(TDRD7):c.1694C>T (p.Pro565Leu) rs148718632 0.00016
NM_014290.3(TDRD7):c.3129T>C (p.His1043=) rs371279564 0.00015
NM_014290.3(TDRD7):c.2257A>G (p.Ile753Val) rs201436824 0.00013
NM_014290.3(TDRD7):c.2267G>A (p.Arg756Gln) rs183885850 0.00013
NM_014290.3(TDRD7):c.854C>T (p.Thr285Met) rs141457141 0.00013
NM_014290.3(TDRD7):c.295C>T (p.Arg99Cys) rs200783564 0.00012
NM_014290.3(TDRD7):c.2080-15A>G rs372316746 0.00011
NM_014290.3(TDRD7):c.*220T>C rs1006051819 0.00008
NM_014290.3(TDRD7):c.579G>A (p.Ala193=) rs75516981 0.00008
NM_014290.3(TDRD7):c.987G>A (p.Pro329=) rs761704668 0.00007
NM_014290.3(TDRD7):c.2039G>T (p.Ser680Ile) rs140111735 0.00006
NM_014290.3(TDRD7):c.2104T>A (p.Ser702Thr) rs946019953 0.00006
NM_014290.3(TDRD7):c.2251A>C (p.Arg751=) rs1171168935 0.00006
NM_014290.3(TDRD7):c.1892A>G (p.Asn631Ser) rs376812712 0.00005
NM_014290.3(TDRD7):c.199T>C (p.Ser67Pro) rs148039648 0.00005
NM_014290.3(TDRD7):c.1261C>A (p.His421Asn) rs112811088 0.00004
NM_014290.3(TDRD7):c.1950C>T (p.Asp650=) rs769740908 0.00004
NM_014290.3(TDRD7):c.2872G>A (p.Ala958Thr) rs751158396 0.00004
NM_014290.3(TDRD7):c.2390A>G (p.Asn797Ser) rs747436777 0.00003
NM_014290.3(TDRD7):c.2679G>A (p.Thr893=) rs144693621 0.00003
NM_014290.3(TDRD7):c.54T>C (p.His18=) rs749676206 0.00003
NM_014290.3(TDRD7):c.700A>G (p.Met234Val) rs758372213 0.00003
NM_014290.3(TDRD7):c.1032A>G (p.Lys344=) rs111320552 0.00002
NM_014290.3(TDRD7):c.1276A>G (p.Ile426Val) rs766673237 0.00002
NM_014290.3(TDRD7):c.2001C>G (p.Leu667=) rs764337688 0.00002
NM_014290.3(TDRD7):c.2285T>C (p.Ile762Thr) rs746282969 0.00002
NM_014290.3(TDRD7):c.2524T>C (p.Trp842Arg) rs1274740363 0.00002
NM_014290.3(TDRD7):c.2605A>G (p.Met869Val) rs757817371 0.00002
NM_014290.3(TDRD7):c.1308G>A (p.Gln436=) rs777608846 0.00001
NM_014290.3(TDRD7):c.223A>G (p.Met75Val) rs769552442 0.00001
NM_014290.3(TDRD7):c.2941A>G (p.Ile981Val) rs763792246 0.00001
NM_014290.3(TDRD7):c.2955A>G (p.Gly985=) rs201216195 0.00001
NM_014290.3(TDRD7):c.3038G>A (p.Arg1013Gln) rs758400042 0.00001
NM_014290.3(TDRD7):c.582C>A (p.Ser194=) rs772250609 0.00001
NM_014290.3(TDRD7):c.637+13A>G rs370507991 0.00001
NM_014290.3(TDRD7):c.718C>T (p.Arg240Cys) rs199787418 0.00001
NM_014290.3(TDRD7):c.-6-3T>C rs747079212
NM_014290.3(TDRD7):c.1105T>G (p.Tyr369Asp)
NM_014290.3(TDRD7):c.1353C>T (p.Asp451=) rs146047308
NM_014290.3(TDRD7):c.1760A>G (p.Asp587Gly) rs1828932238
NM_014290.3(TDRD7):c.1821A>T (p.Glu607Asp) rs1169706990
NM_014290.3(TDRD7):c.207+12A>C rs763703339
NM_014290.3(TDRD7):c.2147G>A (p.Gly716Glu)
NM_014290.3(TDRD7):c.2344A>C (p.Met782Leu) rs752597965
NM_014290.3(TDRD7):c.2344A>G (p.Met782Val)
NM_014290.3(TDRD7):c.2381C>A (p.Ser794Tyr) rs1829105037
NM_014290.3(TDRD7):c.2491A>G (p.Ser831Gly) rs886063214
NM_014290.3(TDRD7):c.2494A>G (p.Ile832Val)
NM_014290.3(TDRD7):c.2603C>T (p.Pro868Leu) rs764446051
NM_014290.3(TDRD7):c.2641C>G (p.Leu881Val)
NM_014290.3(TDRD7):c.2683G>A (p.Ala895Thr)
NM_014290.3(TDRD7):c.2684C>A (p.Ala895Asp)
NM_014290.3(TDRD7):c.3004A>G (p.Ile1002Val) rs202206922
NM_014290.3(TDRD7):c.3010A>G (p.Lys1004Glu)
NM_014290.3(TDRD7):c.3129T>A (p.His1043Gln) rs371279564
NM_014290.3(TDRD7):c.416A>G (p.Asn139Ser) rs1317477843
NM_014290.3(TDRD7):c.692C>G (p.Thr231Ser) rs756033246
NM_014290.3(TDRD7):c.725A>G (p.Lys242Arg) rs1036293350
NM_014290.3(TDRD7):c.838T>C (p.Trp280Arg) rs201246147

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