ClinVar Miner

List of variants studied for cataract 33 by Invitae

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_001195.5(BFSP1):c.1500G>A (p.Ala500=) rs6136118 0.27904
NM_001195.5(BFSP1):c.1926C>T (p.Thr642=) rs6080717 0.26382
NM_001195.5(BFSP1):c.1033G>A (p.Gly345Ser) rs6080719 0.20403
NM_001195.5(BFSP1):c.804C>T (p.Asn268=) rs11537702 0.05390
NM_001195.5(BFSP1):c.1968C>A (p.Asp656Glu) rs16999317 0.01485
NM_001195.5(BFSP1):c.1125G>T (p.Glu375Asp) rs139124891 0.01147
NM_001195.5(BFSP1):c.46G>C (p.Glu16Gln) rs200899362 0.01003
NM_001195.5(BFSP1):c.137G>C (p.Gly46Ala) rs143850362 0.00985
NM_001195.5(BFSP1):c.736-16G>A rs76806936 0.00427
NM_001195.5(BFSP1):c.887C>T (p.Ala296Val) rs142996076 0.00285
NM_001195.5(BFSP1):c.418A>G (p.Met140Val) rs142092768 0.00275
NM_001195.5(BFSP1):c.1995_1996del (p.Ter666LysextTer?) rs548358901 0.00264
NM_001195.5(BFSP1):c.762A>G (p.Lys254=) rs35042144 0.00210
NM_001195.5(BFSP1):c.1148A>G (p.Asn383Ser) rs150798461 0.00099
NM_001195.5(BFSP1):c.1775C>T (p.Ala592Val) rs145703098 0.00069
NM_001195.5(BFSP1):c.403C>T (p.Leu135Phe) rs151173407 0.00065
NM_001195.5(BFSP1):c.675G>A (p.Leu225=) rs140834233 0.00064
NM_001195.5(BFSP1):c.374G>A (p.Ser125Asn) rs561395667 0.00056
NM_001195.5(BFSP1):c.183C>T (p.Leu61=) rs545346553 0.00030
NM_001195.5(BFSP1):c.1936G>A (p.Val646Met) rs145017887 0.00027
NM_001195.5(BFSP1):c.526C>T (p.His176Tyr) rs140135049 0.00027
NM_001195.5(BFSP1):c.812T>C (p.Ile271Thr) rs147718368 0.00026
NM_001195.5(BFSP1):c.1939G>C (p.Glu647Gln) rs148119487 0.00017
NM_001195.5(BFSP1):c.685C>T (p.Arg229Trp) rs372210205 0.00009
NM_001195.5(BFSP1):c.735+9G>A rs774559581 0.00008
NM_001195.5(BFSP1):c.627+9T>G rs776455142 0.00004
NM_001195.5(BFSP1):c.735+17C>T rs368674829 0.00003
NM_001195.5(BFSP1):c.1339A>C (p.Lys447Gln) rs765144287 0.00002
NM_001195.5(BFSP1):c.1468A>G (p.Thr490Ala) rs756439203 0.00002
NM_001195.5(BFSP1):c.1943C>T (p.Thr648Ile) rs752902567 0.00002
NM_001195.5(BFSP1):c.1402G>C (p.Glu468Gln) rs780229198 0.00001
NM_001195.5(BFSP1):c.1437C>T (p.Tyr479=) rs760220303 0.00001
NM_001195.5(BFSP1):c.735+19C>T rs747126284 0.00001
NM_001195.5(BFSP1):c.898C>T (p.Gln300Ter) rs1246080692 0.00001
NC_000020.10:g.(?_17462209)_(17511974_?)dup
NM_001195.5(BFSP1):c.1029A>G (p.Gly343=)
NM_001195.5(BFSP1):c.106_107delinsTT (p.Ala36Phe) rs886038419
NM_001195.5(BFSP1):c.1162G>T (p.Asp388Tyr)
NM_001195.5(BFSP1):c.1286_1287insTGGACACAAGA (p.Glu429fs)
NM_001195.5(BFSP1):c.1332A>G (p.Leu444=)
NM_001195.5(BFSP1):c.136G>T (p.Gly46Trp)
NM_001195.5(BFSP1):c.1406G>A (p.Arg469Gln)
NM_001195.5(BFSP1):c.1678C>T (p.Arg560Cys)
NM_001195.5(BFSP1):c.1749A>G (p.Pro583=) rs6080718
NM_001195.5(BFSP1):c.1749A>T (p.Pro583=) rs6080718
NM_001195.5(BFSP1):c.1876G>A (p.Glu626Lys)
NM_001195.5(BFSP1):c.1884C>T (p.Ile628=)
NM_001195.5(BFSP1):c.1927G>A (p.Ala643Thr)
NM_001195.5(BFSP1):c.1937delinsAA (p.Val646fs) rs1555799947
NM_001195.5(BFSP1):c.205C>T (p.Arg69Trp)
NM_001195.5(BFSP1):c.215T>C (p.Leu72Pro) rs2123536475
NM_001195.5(BFSP1):c.30C>T (p.Thr10=)
NM_001195.5(BFSP1):c.366G>A (p.Glu122=)
NM_001195.5(BFSP1):c.378-16T>C rs1600661739
NM_001195.5(BFSP1):c.384A>G (p.Glu128=)
NM_001195.5(BFSP1):c.452C>G (p.Ala151Gly)
NM_001195.5(BFSP1):c.55G>A (p.Asp19Asn)
NM_001195.5(BFSP1):c.561C>T (p.Ile187=)
NM_001195.5(BFSP1):c.628-14C>T
NM_001195.5(BFSP1):c.658G>A (p.Ala220Thr)
NM_001195.5(BFSP1):c.776_777del (p.Cys259fs)
NM_001195.5(BFSP1):c.847C>T (p.Arg283Trp)
NM_001195.5(BFSP1):c.878G>A (p.Arg293Gln)
NM_001195.5(BFSP1):c.892G>A (p.Ala298Thr)
NM_001195.5(BFSP1):c.93C>A (p.Ala31=)
NM_001195.5(BFSP1):c.956+7G>C rs202146533
NM_001195.5(BFSP1):c.957-3C>T

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