ClinVar Miner

List of variants in gene SPINK5 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_006846.4(SPINK5):c.1480-315C>T rs112385899 0.02835
NM_006846.4(SPINK5):c.3186+200T>C rs41291439 0.02729
NM_006846.4(SPINK5):c.81+206A>G rs73269137 0.01527
NC_000005.10:g.148063880G>A rs2287773 0.01463
NM_006846.4(SPINK5):c.282+269A>G rs79703213 0.01448
NM_006846.4(SPINK5):c.1887+104G>A rs77539681 0.01447
NM_006846.4(SPINK5):c.410+37G>T rs73269187 0.01443
NM_006846.4(SPINK5):c.2965-330G>A rs73271175 0.01419
NM_006846.4(SPINK5):c.282+170T>A rs55752016 0.01389
NM_006846.4(SPINK5):c.2539-321_2539-310del rs1283163411 0.01361
NM_006846.4(SPINK5):c.603-146C>A rs116419684 0.01332
NM_006846.4(SPINK5):c.1479+275C>T rs112355744 0.01164
NM_006846.4(SPINK5):c.1220+210T>A rs78504440 0.01042
NM_006846.4(SPINK5):c.883-177C>T rs146603646 0.01006
NM_006846.4(SPINK5):c.1010+88G>A rs76850452 0.00859
NM_006846.4(SPINK5):c.1608-121T>A rs74393428 0.00747
NM_006846.4(SPINK5):c.56-139T>C rs115476809 0.00702
NM_006846.4(SPINK5):c.1608-172G>C rs116698893 0.00648
NM_006846.4(SPINK5):c.1693-201T>C rs72829100 0.00615
NM_006846.4(SPINK5):c.602+226A>G rs115402328 0.00597
NM_006846.4(SPINK5):c.474+282A>C rs73794659 0.00571
NM_006846.4(SPINK5):c.882+44T>G rs557320665 0.00490
NM_006846.4(SPINK5):c.2739+96T>C rs72831109 0.00434
NM_006846.4(SPINK5):c.1128C>T (p.Asn376=) rs78128189 0.00360
NM_006846.4(SPINK5):c.2739+82T>C rs187199442 0.00346
NM_006846.4(SPINK5):c.3183G>A (p.Pro1061=) rs77756935 0.00345
NM_006846.4(SPINK5):c.2442-16A>G rs148657069 0.00338
NM_006846.4(SPINK5):c.2061G>A (p.Gln687=) rs36111383 0.00336
NM_006846.4(SPINK5):c.666+211G>A rs189675926 0.00313
NM_006846.4(SPINK5):c.1302+16C>T rs112708641 0.00241
NM_006846.4(SPINK5):c.2539-40A>G rs74293395 0.00091
NM_006846.4(SPINK5):c.2124T>C (p.Ala708=) rs200884153 0.00058
NM_006846.4(SPINK5):c.598C>T (p.Leu200=) rs114784178 0.00058
NM_006846.4(SPINK5):c.803G>A (p.Arg268His) rs375727921 0.00035
NM_006846.4(SPINK5):c.1539G>A (p.Glu513=) rs184512279 0.00019
NM_006846.4(SPINK5):c.3189C>T (p.Asp1063=) rs200751535 0.00018
NM_006846.4(SPINK5):c.1431-13C>T rs375240260 0.00005
NM_006846.4(SPINK5):c.1092+201_1092+204del rs3214448
NM_006846.4(SPINK5):c.1607+240del
NM_006846.4(SPINK5):c.1888-93_1888-92insTT rs377089918
NM_006846.4(SPINK5):c.1888-93_1888-92insTTTT rs377089918
NM_006846.4(SPINK5):c.2539-269AT[9] rs145110538
NM_006846.4(SPINK5):c.2539-311TA[14] rs1159209367
NM_006846.4(SPINK5):c.2539-321A>T rs200058292
NM_006846.4(SPINK5):c.2667-16T>G rs1057521635
NM_006846.4(SPINK5):c.81+19G>A rs1057520976

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