ClinVar Miner

List of variants reported as uncertain significance for Senior-Loken syndrome 1

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NC_000002.12:g.110123331A>T
NC_000002.12:g.110205022G>A
NM_000272.3(NPHP1):c.625-3dup rs200118387
NM_000272.4(NPHP1):c.*250C>T rs150558683
NM_000272.4(NPHP1):c.*322A>G rs886054752
NM_000272.4(NPHP1):c.1035A>G (p.Gln345=) rs371112962
NM_000272.4(NPHP1):c.1121C>T (p.Thr374Ile) rs140469160
NM_000272.4(NPHP1):c.1333C>T (p.Arg445Cys) rs375907280
NM_000272.4(NPHP1):c.1447G>C (p.Glu483Gln) rs886054753
NM_000272.4(NPHP1):c.1637G>A (p.Arg546Lys) rs149887461
NM_000272.4(NPHP1):c.1690G>C (p.Val564Leu) rs573192954
NM_000272.4(NPHP1):c.1889C>T (p.Ser630Leu) rs138181219
NM_000272.4(NPHP1):c.1929+5A>C rs201030203
NM_000272.4(NPHP1):c.2029G>C (p.Glu677Gln) rs780427871
NM_000272.4(NPHP1):c.2100C>T (p.Gly700=) rs200631256
NM_000272.4(NPHP1):c.232T>C (p.Tyr78His) rs140446520
NM_000272.4(NPHP1):c.456A>G (p.Ser152=) rs143163969
NM_000272.4(NPHP1):c.460G>A (p.Gly154Ser) rs769509705
NM_000272.4(NPHP1):c.593A>G (p.Asn198Ser) rs886054756
NM_000272.4(NPHP1):c.669C>T (p.Gly223=) rs886054755
NM_000272.4(NPHP1):c.860A>G (p.Asn287Ser) rs139787582
NM_000272.4(NPHP1):c.940-5T>C rs201478764
NM_000272.4(NPHP1):c.969G>A (p.Thr323=) rs141763330
NM_000272.4(NPHP1):c.971T>C (p.Met324Thr) rs114250691
NM_000272.4(NPHP1):c.988G>C (p.Gly330Arg) rs886054754
NM_001128178.3(NPHP1):c.*199A>G
NM_001128178.3(NPHP1):c.*238T>C
NM_001128178.3(NPHP1):c.137A>G (p.Tyr46Cys)
NM_001128178.3(NPHP1):c.1534C>T (p.Leu512=)
NM_001128178.3(NPHP1):c.1693C>A (p.Pro565Thr)
NM_001128178.3(NPHP1):c.1716+15T>C
NM_001128178.3(NPHP1):c.1717-5T>G
NM_001128178.3(NPHP1):c.1804C>G (p.His602Asp)
NM_001128178.3(NPHP1):c.240G>A (p.Gln80=)
NM_001128178.3(NPHP1):c.30C>T (p.Leu10=)
NM_001128178.3(NPHP1):c.352G>A (p.Glu118Lys)
NM_001128178.3(NPHP1):c.771+148G>T
NM_001128178.3(NPHP1):c.771+178C>T

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